Compositions and methods for treating cancer

ABSTRACT

Provided herein are methods of treating cancer comprising administering decitabine in combination with compounds that inhibit the deamination enzyme responsible for the inactivation of decitabine.

RELATED APPLICATION

This application claims priority to U.S. Provisional Application No. 61/167,119, filed Apr. 6, 2009, entitled “COMPOSITIONS AND METHODS FOR TREATING CANCER.” The contents of any patents, patent applications, and references cited throughout this specification are hereby incorporated by reference in their entireties.

BACKGROUND OF THE INVENTION

Cancer is the second most common cause of death in the U.S., exceeded only by heart disease, and accounts for 1 of every 4 deaths. Since 1990, in the U.S. alone, nearly five million lives have been lost to some form of cancer.

For example, breast cancer affects 186,000 women annually in the U.S., and the mortality rate of this disease has remained unchanged for 50 years. Surgical resection of the disease through radical mastectomy, modified radical mastectomy, or lumpectomy remains the mainstay of treatment for this condition. Unfortunately, a high percentage of those treated with lumpectomy alone will develop a recurrence of the disease.

Lung cancer is the most common cause of cancer death in both sexes in the United States. Lung cancer can result from a primary tumor originating in the lung or a secondary tumor which has spread from another organ such as the bowel or breast. Primary lung cancer is divided into three main types; small cell lung cancer; non-small cell lung cancer; and mesothelioma. There are three types of non-small cell lung cancer: squamous cell carcinoma, adenocarcinoma, and large cell carcinoma. Mesothelioma is a rare type of cancer that affects the covering of the lung called the pleura, and is often caused by exposure to asbestos.

Ovarian cancer accounts for about 3% of all cancers among women and ranks second among gynecologic cancers, following cancer of the uterine corpus. Ovarian cancer affects over 20,000 women in the United States each year and causes some 15,000 deaths annually. If the disease is diagnosed at the localized stage, the 5-year survival rate is over 90%; however, only about 19% of all cases are detected at this stage.

The incidence of pancreatic cancer has been increasing steadily in the past twenty years in most industrialized countries, exhibiting the characteristics of a growing epidemiological problem.

Leukemia is a type of cancer that affects blood cells. Among the currently prescribed treatment regimes for leukemia are total body irradiation and chemotherapy. The two treatment regimes, however, pose a clinical dilemma: because leukemia is a cancer of the blood, all of the cells in the blood and all of the cells that arise in bone marrow must be treated in order to ensure destruction of the neoplastic cells. Destruction of all these cells leaves the patient in a severely immunodepressed state which could be as fatal as the leukemia.

Moreover, some cancer drugs are metabolized by an organism's naturally occurring enzymes such as adenosine deaminase (ADA, EC 3.5.4.4) and cytidine deaminase (CDA, also termed cytosine nucleoside deaminase, cytidine aminohydrolase, or EC 3.5.4.5). These enzymes function to deaminate natural aminopurine and aminopyrimidine nucleosides, respectively, in human and other organisms. These enzymes also convert active nucleoside-based cancer drugs into inactive metabolites. For example, the purine nucleoside drug arabinosyladenine (fludarabine, ara-A) is deaminated by ADA; the resulting compound, with the parent amino group replaced with hydroxyl, is inactive as an antitumor agent compared to the parent compound.

CDA is a component of the pyrimidine salvage pathway. It converts cytidine and deoxycytidine to uridine and deoxyuridine, respectively, by hydrolytic deamination (Arch. Biochem. Biophys. 1991, 290, 285-292; Methods Enzymol. 1978, 51, 401-407; Biochem. J. 1967, 104, 7P). It also deaminates a number of synthetic cytosine analogs which are clinically useful drugs (Cancer Chemother. Pharmacol. 1998, 42, 373-378; Cancer Res. 1989, 49, 3015-3019; Antiviral Chem. Chemother. 1990, 1, 255-262). Conversion of the cytosine compounds to the uridine derivatives usually confers loss of therapeutic activity or addition of side-effects. It has also been shown that cancers that acquire resistance to cytosine analog drugs often overexpress CDA (Leuk. Res. 1990, 14, 751-754). Leukemic cells expressing a high level of CDA can manifest resistance to cytosine antimetabolites and thereby limit the antineoplastic activity of such therapeutics (Biochem. Pharmacol. 1993, 45, 1857-1861).

Tetrahydrouridine (THU, or 1(β-D-Ribofuranosyl)-4-hydroxytetrahydropyrimidin-2(1H)-one) has been known as an inhibitor of cytidine deaminase for a number of years.

Various reports have suggested that co-administration with THU increases the efficacy and oral activity of cytidine-based drugs. See, e.g., Cancer Chemotherapy Reports 1975, 59, 459-465 and Blood 1985, 66, 527-532. However, early CDA inhibitors such as THU suffer from drawbacks that include acid instability (J. Med. Chem. 1986, 29, 2351) and poor bioavailability (J. Clin. Pharmacol. 1978, 18, 259).

5-Aza-2′-deoxycytidine (also termed decitabine; or, the active agent in the branded product Dacogen®) is an antineoplastic agent for the treatment of myelodysplastic syndrome (MDS), with potential utility for the treatment of AML and CML as well. Like the other cytidine-based drugs, its oral bioavailability and efficacy are limited by deactivation by CDA. THU has been shown to improve the potency of decitabine in a sickle cell disease model in baboons (Am. J. Hematol. 1985, 18, 283-288). In addition, another known CDA inhibitor, zebularine, has been shown to enhance the efficacy of decitabine in mice with L1210 leukemia (Anticancer Drugs 2005, 16, 301-308).

There is therefore an ongoing need for new, potent and therapeutically useful inhibitors of CDA that can be used with decitabine for treating cancer or neoplastic disease.

SUMMARY OF THE INVENTION

There remains a need for new treatments and therapies for cancer and cancer-associated disorders. There is also a need for compounds useful in the treatment or amelioration of one or more symptoms of cancer. Furthermore, there is a need for methods for inhibiting the activity of the enzyme cytidine deaminase.

Thus, provided herein are compositions comprising (i) decitabine and (ii) a compound of formula I, II, III, IV, V, VI, VII, or VIII, or pharmaceutically acceptable salts, C₁₋₆ alkyl esters, or C₂₋₆ alkenyl esters thereof. In one aspect of the invention, provided herein are compositions comprising (i) decitabine and (ii) a compound of formula VIII, or pharmaceutically acceptable salts, C₁₋₆ alkyl esters, or C₂₋₆ alkenyl esters thereof. In another aspect, provided herein is a method of treating cancer comprising administering to a subject a composition comprising decitabine; and administering to a subject a composition comprising a compound of formula I, II, III, IV, V, VI, VII, or VIII, or pharmaceutically acceptable salts, C₁₋₆ alkyl esters, or C₂₋₆ alkenyl esters thereof.

In another aspect, provided herein is a method of treating cancer comprising administering to a subject a composition comprising decitabine, and administering to a subject a composition comprising a compound of formula I, or pharmaceutically acceptable salts, C₁₋₆ alkyl esters, or C₂₋₆ alkenyl esters thereof. In one embodiment of this method, the composition comprising decitabine and the composition comprising a compound of formula I are simultaneously administered. In another embodiment, the composition comprising decitabine and the composition comprising a compound of formula I are sequentially administered.

In another aspect, provided herein is a method of treating cancer comprising administering to a subject a composition comprising decitabine; and administering to a subject a composition comprising a compound of formula VIII, or pharmaceutically acceptable salts, C₁₋₆ alkyl esters, or C₂₋₆ alkenyl esters thereof. In one embodiment of this method, the composition comprising decitabine and the composition comprising a compound of formula VIII are simultaneously administered. In another embodiment, the composition comprising decitabine and the composition comprising a compound of formula VIII are sequentially administered.

In another aspect, provided herein are pharmaceutical compositions comprising (i) decitabine; (ii) a compound of formula I, II, III, IV, V, VI, VII, or VIII, or pharmaceutically acceptable salts, C₁₋₆ alkyl esters, or C₂ alkenyl esters thereof; and (iii) a pharmaceutically acceptable excipient.

In another aspect, provided herein are pharmaceutical compositions comprising (i) decitabine; (ii) a compound of formula VIII, or pharmaceutically acceptable salts, C₁₋₆ alkyl esters, or C₂₋₆ alkenyl esters thereof; and (iii) a pharmaceutically acceptable excipient. In any of these embodiments, the cancer may be a hematological cancer or solid cancer. The hematological cancer may be myelodysplastic syndrome or leukemia. The leukemia may be acute myeloid leukemia or chronic myeloid leukemia. The solid cancer may be pancreatic cancer, ovarian cancer, peritoneal cancer, non small cell lung cancer, or metastatic breast cancer.

In another aspect, provided herein is a method of treating cancer comprising administering to a subject a pharmaceutical composition comprising decitabine; and administering to a subject a pharmaceutical composition comprising a compound of formula VIII, or a pharmaceutically acceptable salt, a C₁₋₆ alkyl ester, or a C₂₋₆ alkenyl ester thereof; and a pharmaceutically acceptable carrier.

In one embodiment, the cancer is a hematological cancer or solid cancer. The hematological cancer can be myelodysplastic syndrome or leukemia. The leukemia can be acute myeloid leukemia or chronic myeloid leukemia. The solid cancer can be pancreatic cancer, ovarian cancer, peritoneal cancer, non small cell lung cancer, or metastatic breast cancer.

In yet another aspect, provided herein is a use of the compound of formula I, or a pharmaceutically acceptable salt, a C₁₋₆ alkyl ester, or a C₂₋₆ alkenyl ester thereof; for the manufacture of a medicament for treating cancer in a subject being treated with a composition comprising decitabine.

In one embodiment, the cancer is a hematological cancer or solid cancer. The hematological cancer can be myelodysplastic syndrome or leukemia. The leukemia can be acute myeloid leukemia or chronic myeloid leukemia. The solid cancer can be pancreatic cancer, ovarian cancer, peritoneal cancer, non small cell lung cancer, or metastatic breast cancer.

In still another aspect, provided herein is a use of the compound of formula VIII, or a pharmaceutically acceptable salt, a C₁₋₆ alkyl ester, or a C₂₋₆ alkenyl ester thereof;

for the manufacture of a medicament for treating cancer in a subject being treated with a composition comprising decitabine. In one embodiment, the cancer is a hematological cancer or solid cancer. The hematological cancer can be myelodysplastic syndrome or leukemia. The leukemia can be acute myeloid leukemia or chronic myeloid leukemia. The solid cancer can be pancreatic cancer, ovarian cancer, peritoneal cancer, non small cell lung cancer, or metastatic breast cancer.

In another aspect, provided herein is a method of preventing the deamination of decitabine, which comprises utilizing an effective amount of any compound of the formulae I-VIII. In a particular embodiment of this method, the compound is a compound given by formula VIII.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows a plot of total HPLC area-% purities of ER-876400 (1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-3,4-dihydro-1H-1,3-diazepin-2(7H)-one) as a function of time in simulated gastric fluid at 37° C.

FIG. 2 shows a plot of total HPLC area-% purities of ER-876437 (1-((2R,4R,5R)-3,3-difluoro-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-3,4-dihydro-1H-1,3-diazepin-2(7H)-one) as a function of time in simulated gastric fluid at 37° C.

FIG. 3 shows the UV Spectrum of decitabine and ER-876437.

FIG. 4 shows the HPLC chromatograms of decitabine in the presence of CDA in Tris-HCl buffer at 37° C. at selected time points.

FIG. 5 shows the HPLC chromatograms of decitabine in the presence of CDA and ER-876437 in Tris-HCl buffer at 37° C. at selected time points.

FIG. 6 shows the effect of ER-876437 on the levels of decitabine in the presence of CDA in Tris-HCl buffer at 37° C.

DETAILED DESCRIPTION OF THE INVENTION

Enzymes that deaminate natural aminopurine and aminopyrimidine nucleosides can also convert active anti-cancer drugs into inactive compounds in the human body. For example, the enzyme cytidine deaminase can rapidly convert the amino group of certain drugs to a hydroxyl group, rendering these compounds inactive. When an inhibitor of cytidine deaminase is co-administered with a drug that is otherwise deaminated (and consequently deactivated) by this enzyme, improved anti-tumor activity will be achieved.

The cytidine deaminase inhibitor (Z)-3,4-dihydro-1-((2R,3R,4S,5R)-tetrahydro-3,4-dihydroxy-5-(hydroxymethyl)furan-2-yl)-1H-1,3-diazepin-2(7H)-one (also referred to herein as “ER-876400”; 1-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-3,4-dihydro-1H-1,3-diazepin-2(7H)-one; 2H-1,3-Diazepin-2-one, 1,3,4,7-tetrahydro-1-β-D-ribofuranosyl-; or given by chemical registry no. 75421-11-3) has been described in Liu, P. S. et al., J. Med. Chem. 24:662-666 (1981); and in U.S. Pat. No. 4,275,057 (both of which are incorporated herein by reference in their entireties). ER-876400 is given by formula IX:

(Here and elsewhere, where discrepancies exist between a compound's name and a compound's structure, the chemical structure will control.)

Other cytidine deaminase inhibitors have previously been described in international application no. PCT/US2008/80163, filed on Oct. 16, 2008; in U.S. patent application Ser. No. 12/252,961, filed on Oct. 16, 2008; and in U.S. provisional patent application No. 60/980,397, filed Oct. 16, 2007; all of which are hereby incorporated by reference in their entireties.

Provided herein is a new class of inhibitors of cytidine deaminase (“CDA”). As described herein, these compounds have an improved half-life over other known compounds. In one embodiment, the compounds of the invention have an improved half-life in simulated gastric fluid compared to ER-876400. These compounds can be administered in combination with decitabine for purposes of treating cancer (e.g., myelodysplastic syndrome, leukemia, pancreatic cancer, ovarian cancer, peritoneal cancer, non small cell lung cancer, or metastatic breast cancer).

DEFINITIONS

The following definitions are used throughout this specification:

As used in the specification and claims, the singular forms “a,” “an,” and “the” include plural references unless the content clearly dictates otherwise. Thus, for example, reference to a pharmaceutical composition comprising “a compound” may encompass two or more compounds.

The term “decitabine,” the active agent in the branded drug known as “DACOGEN®” or “5-aza-2′-deoxycytidine” refers to a compound having the formula:

“Alkyl” or “alkyl group” as used herein, means a straight-chain (i.e., unbranched), branched, or cyclic hydrocarbon chain that is completely saturated. Examples include without limitation methyl, ethyl, propyl, iso-propyl, butyl, iso-butyl, tert-butyl, n-pentyl and n-hexyl. In some embodiments, the alkyl chain is a C₁ to C₆ branched or unbranched carbon chain. In some embodiments, the alkyl chain is a C₂ to C₅ branched or unbranched carbon chain. In some embodiments, the alkyl chain is a C₁ to C₄ branched or unbranched carbon chain. In some embodiments, the alkyl chain is a C₂ to C₄ branched or unbranched carbon chain. In some embodiments, the alkyl chain is a C₃ to C₅ branched or unbranched carbon chain. In some embodiments, the alkyl chain is a C₁ to C₂ carbon chain. In some embodiments, the alkyl chain is a C₂ to C₃ branched or unbranched carbon chain. “In certain embodiments, the term “alkyl” or “alkyl group” includes a cycloalkyl group, also known as a carbocycle. Exemplary C₁₋₃ alkyl groups include methyl, ethyl, propyl, isopropyl, and cyclopropyl.

“Alkenyl” or “alkenyl group,” as used herein, refers to a straight-chain (i.e., unbranched), branched, or cyclic hydrocarbon chain that has one or more double bonds. Examples include without limitation ethenyl, propenyl, iso-propenyl, butenyl, iso-butenyl, tert-butenyl, n-pentenyl and n-hexenyl. In some embodiments, the alkenyl chain is a C₂ to C₆ branched or unbranched carbon chain. In some embodiments, the alkenyl chain is a C₂ to C₅ branched or unbranched carbon chain. In some embodiments, the alkenyl chain is a C₂ to C₄ branched or unbranched carbon chain. In some embodiments, the alkenyl chain is a C₃ to C₅ branched or unbranched carbon chain. According to another aspect, the term alkenyl refers to a straight chain hydrocarbon having two double bonds, also referred to as “diene.” In other embodiments, the term “alkenyl” or “alkenyl group” refers to a cycloalkenyl group.

“C₁₋₆ alkyl ester” refers to a C₁₋₆ alkyl ester where each C₁₋₆ alkyl group is as defined above. Accordingly, a C₁₋₆ alkyl ester group of an alcohol (—OH) has the formula —C(═O)O(C₁₋₆ alkyl), wherein the terminal oxygen occupies the position of the alcoholic oxygen.

“C₂₋₆ alkenyl ester” refers to a C₂₋₆ alkenyl ester where each C₂₋₆ alkenyl group is as defined above. Accordingly, a C₂₋₆ alkenyl ester group of an alcohol (—OH) has the formula —C(═O)O(C₂₋₆ alkenyl), wherein the terminal oxygen occupies the position of the alcoholic oxygen.

Unless indicated otherwise, where a bivalent group is described by its chemical formula, including two terminal bond moieties indicated by “-,” it will be understood that the attachment is read from left to right.

Unless stereochemistry is depicted or otherwise stated or shown, structures depicted herein are also meant to include all enantiomeric, diastereomeric, and geometric (or conformational) forms of the structure; for example, the R and S configurations for each asymmetric center, (Z) and (E) double bond isomers, and (Z) and (E) conformational isomers. Therefore, single stereochemical isomers as well as enantiomeric, diastereomeric, and geometric (or conformational) mixtures of the present compounds are within the scope of the invention. Any tautomeric forms of the compounds of the invention are within the scope of the invention.

Additionally, unless otherwise stated, structures depicted herein are also meant to include compounds that differ only in the presence of one or more isotopically enriched atoms. For example, compounds having the present structures except for the replacement of hydrogen by deuterium or tritium, or the replacement of a carbon by a ¹³C- or ¹⁴C-enriched carbon are within the scope of this invention. Such compounds are useful, for example, as analytical tools or probes in biological assays.

“Treatment,” “treat,” and “treating” refer to reversing, alleviating, delaying the onset of, or inhibiting the progress of a disease or disorder as described herein. In some embodiments, treatment may be administered after one or more symptoms have developed. In other embodiments, treatment may be administered in the absence of symptoms. For example, treatment may be administered to a susceptible individual prior to the onset of symptoms (e.g., in light of a history of symptoms or in light of genetic or other susceptibility factors, or in light of a history of symptoms and in light of genetic or other susceptibility factors). Treatment may also be continued after symptoms have resolved, for example to mitigate or delay their recurrence. “Treating” in reference to a disease, disorder or condition also refers to: (i) slowing a disease, disorder or condition, e.g., arresting its development; or (ii) relieving a disease, disorder or condition, e.g., causing regression of the clinical symptoms, or (iii) slowing a disease, disorder or condition and relieving a disease, disorder or condition.

“Preventing” in reference to a disease, disorder or condition refers to preventing a disease, disorder or condition, e.g., causing the clinical symptoms of the disease, disorder or condition not to develop.

“Inhibit,” “inhibitor,” and “inhibition” in reference to any of the compounds given by formulae I VIII (or the CDA inhibitors described herein including without limitation any of their salts, alkyl esters or alkenyl esters) refers to reducing the ability of CDA to bind a decitabine, thereby reducing the ability of CDA to enzymatically deaminate decitabine. Without being bound by any theory, a compound's ability to inhibit CDA can be due to the compound's ability to bind the active site of a particular CDA protein thereby reducing the ability of that particular CDA protein from binding decitabine. “Inhibit,” “inhibitor,” and “inhibition” in this context does not refer to a complete prevention of all CDA proteins from binding decitabine. Rather, in this context, “inhibit,” “inhibitor,” and “inhibition” relate to the ability of CDA inhibitors to reduce the enzymatic deamination of decitabine by CDA. In one aspect, the methods of the present invention comprise contacting a cell with an effective amount of a CDA inhibitor compound, i.e., a compound of the invention, thereby inhibiting the activity of CDA.

“Patient” or “subject”, as used herein, means an animal subject, preferably a mammalian subject (e.g., dog, cat, horse, cow, sheep, goat, monkey, etc.), and particularly human subjects (including both male and female subjects, and including neonatal, infant, juvenile, adolescent, adult and geriatric subjects). “Subject” can also refer to a cell or tissue, in vitro or in vivo, of an animal or a human.

By the term “combination” is meant either a fixed combination in one dosage unit form, or a kit of parts for the combined administration where a compound of the present invention and a combination partner may be administered independently, at the same time, or separately within time intervals that especially allow that the combination partners show a cooperative, e.g., additive or synergistic, effect, or any combination thereof.

“Pharmaceutically acceptable” refers to those properties or substances that are acceptable to the patient from a pharmacological or toxicological point of view, or to the manufacturing pharmaceutical chemist from a physical or chemical point of view regarding composition, formulation, stability, patient acceptance, bioavailability and compatibility with other ingredients.

“Pharmaceutically acceptable excipient” can mean any substance, not itself a therapeutic agent, used as a carrier, diluent, binder, or vehicle for delivery of a therapeutic agent to a subject, or added to a pharmaceutical composition to improve its handling or storage properties or to permit or facilitate formation of a compound or composition into a unit dosage form for administration. Pharmaceutically acceptable excipients are well known in the pharmaceutical arts and are described, for example, in Remington's Pharmaceutical Sciences, Mack Publishing Co., Easton, Pa. (e.g., 20^(th) Ed., 2000), and Handbook of Pharmaceutical Excipients, American Pharmaceutical Association, Washington, D.C., (e.g., 1^(st), 2^(nd) and 3^(rd) Eds., 1986, 1994 and 2000, respectively). Excipients may provide a variety of functions and may be described as wetting agents, buffering agents, suspending agents, lubricating agents, emulsifiers, disintegrants, absorbents, preservatives, surfactants, colorants, flavorants, and sweeteners. Examples of pharmaceutically acceptable excipients include without limitation: (1) sugars, such as lactose, glucose and sucrose; (2) starches, such as corn starch and potato starch; (3) cellulose and its derivatives, such as sodium carboxymethyl cellulose, ethyl cellulose, cellulose acetate, hydroxypropylmethylcellulose, and hydroxypropylcellulose; (4) powdered tragacanth; (5) malt; (6) gelatin; (7) talc; (8) excipients, such as cocoa butter and suppository waxes; (9) oils, such as peanut oil, cottonseed oil, safflower oil, sesame oil, olive oil, corn oil and soybean oil; (10) glycols, such as propylene glycol; (11) polyols, such as glycerin, sorbitol, mannitol and polyethylene glycol; (12) esters, such as ethyl oleate and ethyl laurate; (13) agar; (14) buffering agents, such as magnesium hydroxide and aluminum hydroxide; (15) alginic acid; (16) pyrogen-free water; (17) isotonic saline; (18) Ringer's solution; (19) ethyl alcohol; (20) pH buffered solutions; (21) polyesters, polycarbonates or polyanhydrides; and (22) other non-toxic compatible substances employed in pharmaceutical formulations.

“Pharmaceutically acceptable carrier” as used herein refers to a nontoxic carrier or vehicle that does not destroy the pharmacological activity of the compound with which it is formulated. Pharmaceutically acceptable carriers or vehicles that may be used in the compositions of this invention include, but are not limited to, ion exchangers, alumina, aluminum stearate, lecithin, serum proteins, such as human serum albumin, buffer substances such as phosphates, glycine, sorbic acid, potassium sorbate, partial glyceride mixtures of saturated vegetable fatty acids, water, salts or electrolytes, such as protamine sulfate, disodium hydrogen phosphate, potassium hydrogen phosphate, sodium chloride, zinc salts, colloidal silica, magnesium trisilicate, polyvinyl pyrrolidone, cellulose-based substances, polyethylene glycol, cyclodextrins, sodium carboxymethylcellulose, polyacrylates, waxes, polyethylene-polyoxypropylene-block polymers, polyethylene glycol and wool fat.

“Pharmaceutically acceptable salt” refers to an acid or base salt of a compound of the invention, which salt possesses the desired pharmacological activity and is neither biologically nor otherwise undesirable. The salt can be formed with acids that include without limitation acetate, adipate, alginate, aspartate, benzoate, benzenesulfonate, bisulfate butyrate, citrate, camphorate, camphorsulfonate, cyclopentanepropionate, digluconate, dodecylsulfate, ethanesulfonate, fumarate, glucoheptanoate, glycerophosphate, hemisulfate, heptanoate, hexanoate, hydrochloride hydrobromide, hydroiodide, 2-hydroxyethane-sulfonate, lactate, maleate, methanesulfonate, 2-naphthalenesulfonate, nicotinate, oxalate, thiocyanate, tosylate and undecanoate. Examples of a base salt include without limitation ammonium salts, alkali metal salts such as sodium and potassium salts, alkaline earth metal salts such as calcium and magnesium salts, salts with organic bases such as dicyclohexylamine salts, N-methyl-D-glucamine, and salts with amino acids such as arginine and lysine. In some embodiments, the basic nitrogen-containing groups can be quarternized with agents including lower alkyl halides such as methyl, ethyl, propyl and butyl chlorides, bromides and iodides; dialkyl sulfates such as dimethyl, diethyl, dibutyl and diamyl sulfates; long chain halides such as decyl, lauryl, myristyl and stearyl chlorides, bromides and iodides; and aralkyl halides such as phenethyl bromides.

“Animal” refers to a living organism having sensation and the power of voluntary movement, and which requires for its existence oxygen and organic food.

“Mammal” refers to a warm-blooded vertebrate animal with hair or fur. Examples include without limitation members of the human, equine, porcine, bovine, murine, canine or feline species.

“Cancer” refers to an abnormal growth of cells which tend to proliferate in an uncontrolled way and, in some cases, to metastasize (spread). Specific cancers types include without limitation the cancers identified in Publication No. US 2006/0014949 and the following:

-   -   cardiac: sarcoma (e.g., such as angiosarcoma, fibrosarcoma,         rhabdomyosarcoma, liposarcoma and the like), rhabdomyoma and         teratoma;     -   lung: bronchogenic carcinoma (e.g., such as squamous cell,         undifferentiated small cell, undifferentiated large cell,         adenocarcinoma and the like), alveolar (e.g., such as         bronchiolar) carcinoma, sarcoma, lymphoma, non-small cell lung         cancer and mesothelioma;     -   gastrointestinal: esophagus (e.g., such as squamous cell         carcinoma, adenocarcinoma, leiomyosarcoma, lymphoma and the         like), stomach (e.g., such as carcinoma, lymphoma,         leiomyosarcoma and the like), pancreas (e.g., such as ductal         adenocarcinoma, insulinoma, carcinoid tumors, vipoma and the         like), small bowel (e.g., such as adenocarcinoma, lymphoma,         carcinoid tumors, Karposi's sarcoma, and the like), large bowel         (e.g., such as adenocarcinoma, and the like);     -   genitourinary tract: kidney (e.g., such as adenocarcinoma,         lymphoma, leukemia, and the like), bladder and urethra (e.g.,         such as squamous cell carcinoma, transitional cell carcinoma,         adenocarcinoma and the like), prostate (e.g., such as         adenocarcinoma, sarcoma), testis (e.g., such as seminoma,         teratoma, embryonal carcinoma, teratocarcinoma, choriocarcinoma,         sarcoma, interstitial cell carcinoma, and the like);     -   liver: hepatoma (e.g., hepatocellular carcinoma and the like),         cholangiocarcinoma, hepatoblastoma, and angiosarcoma;     -   bone: osteogenic sarcoma (e.g., such as osteosarcoma and the         like), fibrosarcoma, malignant fibrous histiocytoma,         chondrosarcoma, Ewing's sarcoma, malignant lymphoma (e.g., such         as reticulum cell sarcoma), multiple myeloma, malignant giant         cell tumor chordoma (e.g., such as osteocartilaginous         exostoses), chondroblastoma, and giant cell tumors;     -   nervous system: skull, meninges (e.g., such as meningiosarcoma,         gliomatosis and the like), brain (e.g., such as astrocytoma,         medulloblastoma, glioma, ependymoma, germinoma [pinealoma],         glioblastoma multiform, oligodendroglioma, retinoblastoma,         congenital tumors and the like), spinal cord (e.g., such as         sarcoma and the like);     -   breast cancer;     -   gynecological: uterus (e.g., such as endometrial carcinoma and         the like), cervix (e.g., such as cervical carcinoma, and the         like), ovaries (e.g., such as ovarian carcinoma [serous         cystadenocarcinoma, mucinous cystadenocarcinoma, unclassified         carcinoma], Sertoli-Leydig cell tumors, dysgerminoma, malignant         teratoma, and the like), vulva (e.g., such as squamous cell         carcinoma, intraepithelial carcinoma, adenocarcinoma,         fibrosarcoma, melanoma and the like), vagina (e.g., such as         clear cell carcinoma, squamous cell carcinoma, botryoid sarcoma         (embryonal rhabdomyosarcoma], fallopian tubes (carcinoma) and         the like);     -   hematologic: blood (e.g., such as myeloid leukemia [acute and         chronic], acute lymphoblastic leukemia, chronic lymphocytic         leukemia, chronic myelocytic leukemia, myeloproliferative         diseases, multiple myeloma, myelodysplastic syndrome and the         like), Hodgkin's disease, non-Hodgkin's lymphoma;     -   skin: malignant melanoma, basal cell carcinoma, squamous cell         carcinoma, Karposi's sarcoma, and the like; and     -   adrenal glands: neuroblastoma.

As used herein, “therapeutically effective amount” refers to an amount sufficient to elicit the desired biological response. A therapeutically effective amount of decitabine, for example, is an amount sufficient to treat a disease or disorder as described herein. A therapeutically effective amount of a compound given by formulae I-VIII is an amount sufficient to increase the in vivo exposure of decitabine.

Throughout the specification, where discrepancies exist between the named compound and the structure shown, the structure shall control. Where any named synonyms (e.g., abbreviations, IUPAC names, generic or other chemic names, or registry numbers) provided for any particular compound actually relate to different compounds, then the specification shall be construed to refer to these compounds in the alternative.

COMPOUNDS OF THE INVENTION

The present invention provides compounds that inhibit the activity of CDA. In another embodiment, these compounds can be administered in combination with decitabine for purposes of treating cancer (e.g., myelodysplastic syndrome, acute myelogenous leukemia, chronic myelocytic leukemia, non-small cell lung cancer, pancreatic cancer, ovarian cancer and breast cancer).

The present invention is directed to a pharmaceutical composition comprising decitabine and a compound of formula I:

wherein:

one of R₁ and R₂ is F, and the other is selected from H and F;

one of R₃ and R₄ is H, and the other is selected from H and OH;

where

is a covalent bond or absent, and R₄ is absent and R₃ is flat when

is a covalent bond;

or a pharmaceutically acceptable salt, a C₁₋₆ alkyl ester, or a C₂₋₆ alkenyl ester thereof.

As used throughout the specification, the expression “R₃ is flat” means that R₃ resides in the same plane as the plane containing the carbon to which R₃ is attached as well as the two carbon atoms immediately adjacent to the carbon to which R₃ is attached.

In one embodiment of formula I, R₁ and R₂ are each F.

In another embodiment, the present invention is directed to a pharmaceutical composition comprising decitabine and a compound of formula II:

or a pharmaceutically acceptable salt, a C₁₋₆ alkyl ester, or a C₂₋₆ alkenyl ester thereof.

In another aspect, the present invention is directed to a pharmaceutical composition comprising decitabine and ER-876437 (or, 2H-1,3-Diazepin-2-one, 1,3,4,7-tetrahydro-1-β-(D-2-deoxy-2,2-difluororibofuranosyl)-; or 1-((2R,4R,5R)-3,3-difluoro-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-3,4-dihydro-1H-1,3-diazepin-2(7H)-one, shown as formula VIII). Here and elsewhere, where discrepancies exist between a compound's chemical name and its structural depiction, the structural depiction will control. Where discrepancies exist between the structural depiction and ¹H NMR data, the ¹H NMR data will control.

In another aspect, the present invention is directed to a pharmaceutical composition comprising decitabine and a compound of formula VIII:

or a pharmaceutically acceptable salt, a C₁₋₆ alkyl ester, or a C₂₋₆ alkenyl ester thereof.

In another aspect, the present invention is directed to a pharmaceutical composition comprising decitabine and a compound of formula VIII:

In another embodiment, the present invention is directed to a pharmaceutical composition comprising decitabine and a compound of formula III:

wherein: one of R₃ and R₄ is H, and the other is selected from H and OH; or a pharmaceutically acceptable salt, a C₁₋₆ alkyl ester, or a C₂₋₆ alkenyl ester thereof.

In another embodiment, the present invention is directed to a pharmaceutical composition comprising decitabine and a compound of formula IV:

or a pharmaceutically acceptable salt, a C₁₋₆ alkyl ester, or a C₂₋₆ alkenyl ester thereof.

In one embodiment, the present invention is directed to a pharmaceutical composition comprising decitabine and a compound of formula V:

or a pharmaceutically acceptable salt, a C₁₋₆ alkyl ester, or a C₂₋₆ alkenyl ester thereof.

In another embodiment, the present invention is directed to a pharmaceutical composition comprising decitabine and a compound of formula VI:

or a pharmaceutically acceptable salt, a C₁₋₆ alkyl ester, or a C₂₋₆ alkenyl ester thereof.

In another embodiment, the present invention is directed to a pharmaceutical composition comprising decitabine and a compound of formula VII:

or a pharmaceutically acceptable salt, a C₁₋₆ alkyl ester, or a C₂₋₆ alkenyl ester thereof.

In another embodiment of the invention, a pharmaceutical composition can comprise (a) a compound of any one of formulae I-VIII and also (b) decitabine.

Another embodiment of the invention is directed to methods of administering the pharmaceutical compositions described herein. Hence, the present invention is directed to a method of treating a subject for cancer comprising administering to the subject decitabine; and administering to the subject a pharmaceutical composition comprising a compound of any one of formulae I-VIII. The decitabine and the compound given can be any one of formulae I-VIII and can be administered to the subject sequentially or simultaneously. A sequential administration includes (a) first administering decitabine followed by (b) administering the pharmaceutical composition comprising a compound of any one of formulae I-VIII. An alternative sequential administration includes (a) first administering the pharmaceutical composition comprising a compound of any one of formulae I-VIII followed by (b) administering decitabine. A simultaneous administration includes administering decitabine and the pharmaceutical composition comprising a compound of any one of formulae I-VIII at the same time; or at substantially the same time.

When administration involves the separate administration (e.g., sequential administration) of the first compound (e.g., a compound of Formula I) and a second compound (e.g., decitabine), as described herein, the compounds are administered sufficiently close in time to have the desired therapeutic effect. For example, the period of time between each administration, which can result in the desired therapeutic effect, can range from minutes to hours to days and can be determined based on the properties of each compound such as potency, solubility, bioavailability, plasma half-life and kinetic profile. For example, the compounds can be administered in any order within 24-72 hours of each other or within any time less than 24 hours of each other. Alternatively, the compounds can be administered in any order within one week of each other.

When decitabine and the compound of any one of formulae I-VIII are administered sequentially, they are separately formulated and can be provided in any order. When decitabine and the compound of any one of formulae I-VIII are administered simultaneously, however, they may be either separately formulated or combined in the same formulation. When combined in the same formulation, decitabine and the compound of any one of formulae I-VIII can be formulated so as to be released into the subject at the same time or at different times. The release profile of a formulation comprising both decitabine and the compound of any one of formulae I-VIII includes the following:

-   -   A) release and bioavailability of decitabine followed by release         and bioavailability of the compound of any one of formulae         I-VIII;     -   B) release and bioavailability of the compound of any one of         formulae I-VIII followed by release and bioavailability of         decitabine;     -   C) release and bioavailability of the compound of any one of         formulae I-VIII at the same time as (or substantially at the         same time as) release and bioavailability of decitabine.

Thus, provided herein is a method of treating cancer, comprising administering to a subject in need thereof a composition comprising decitabine and a compound of any one of formulae I-VIII. The cancer to be treated can be chronic myelocytic leukemia, melanoma, myelodysplasia, relapsed leukemia, colon cancer (including colorectal cancer), gastrointestinal cancer, ovarian cancer, acute lymphoid leukemia, acute myeloid leukemia, lymphocytic leukemia, carcinoma of the prostate, chronic myeloid leukemia, colorectal cancer, non-small cell lung cancer, prostate tumor, renal cell carcinoma, testicular cancer, breast cancer, fallopian tube cancer, ovary tumor, peritoneal tumor, neuroblastoma, non-Hodgkin's lymphoma, head and neck tumor, small intestine cancer, esophagus tumor, lung tumor (or, lung cancer), small cell lung cancer, or mesothelioma. In a particular embodiment, the cancer to be treated is myelodysplastic syndrome, acute myelogenous leukemia, or chronic myelocytic leukemia.

In another embodiment, provided herein is a method of treating cancer in a subject in need thereof, comprising administering to the subject a composition comprising decitabine and ER-876437. In still another embodiment, provided herein is a method of treating cancer in a subject in need thereof, comprising administering to the subject a composition comprising decitabine and ER-876437, wherein the cancer is selected from the group consisting of myelodysplastic syndrome, leukemia, pancreatic cancer, ovarian cancer, peritoneal cancer, non small cell lung cancer, and metastatic breast cancer. In still another embodiment, provided herein is a method of treating acute myelogenous leukemia, myelodysplastic syndrome or chronic myelocytic leukemia in a subject in need thereof, comprising administering to the subject a composition comprising decitabine and ER-876437.

In still another embodiment, provided herein is a method of treating sickle cell anemia in a subject in need thereof, comprising administering to the subject a composition comprising decitabine and ER-876437. In still another embodiment, provided herein is a method of treating postallogeneic progenitor cell transplant relapse in a subject in need thereof, comprising administering to the subject a composition comprising decitabine and ER-876437.

In another embodiment of the invention, the decitabine and the compound of any one of formulae I-VIII can be administered sequentially (in any order) or simultaneously with other pharmaceutical agents typically administered to subjects being treated for cancer. Such other pharmaceutical agents include without limitation anti-emetics, agents that increase appetite, other cytotoxic or chemotherapeutic agents, and agents that relieve pain. The decitabine and the compound of any one of formulae I-VIII can be formulated together with or separately from such other pharmaceutical agents.

A combination with such other pharmaceutical agents can either result in synergistic increase in anti-cancer activity, or such an increase can be additive. Compositions described herein typically include lower dosages of each compound in a composition, thereby avoiding adverse interactions between compounds or harmful side effects, such as ones which have been reported for similar compounds. Furthermore, normal amounts of each compound when given in combination could provide for greater efficacy in subjects who are either unresponsive or minimally responsive to each compound when used alone.

A synergistic effect can be calculated, for example, using suitable methods such as the Sigmoid-Emax equation (Holford, N. H. G. and Scheiner, L. B., Clin. Pharmacokinet. 6: 429-453 (1981)), the equation of Loewe additivity (Loewe, S, and Muischnek, H., Arch. Exp. Pathol Pharmacol. 114: 313-326 (1926)) and the median-effect equation (Chou, T. C. and Talalay, P., Adv. Enzyme Regul. 22: 27-55 (1984)). Each equation referred to above can be applied to experimental data to generate a corresponding graph to aid in assessing the effects of the drug combination. The corresponding graphs associated with the equations referred to above are the concentration-effect curve, isobologram curve and combination index curve, respectively.

In certain embodiments, the invention provides a pharmaceutical composition of any of the compositions of the present invention. In a related embodiment, the invention provides a pharmaceutical composition of any of the compositions of the present invention and a pharmaceutically acceptable carrier or excipient of any of these compositions. In certain embodiments, the invention includes the compositions as novel chemical entities.

In one embodiment, the invention includes a packaged cancer treatment. The packaged treatment includes a composition of the invention packaged with instructions for using an effective amount of the composition of the invention for an intended use. In other embodiments, the present invention provides a use of any of the compositions of the invention for manufacture of a medicament to treat cancer infection in a subject.

Synthetic Procedure

Within the scope of this text, a readily removable group that is not a constituent of the particular desired end product of the compounds of the present invention is designated a “protecting group.” The protection of functional groups by such protecting groups, the protecting groups themselves, and their cleavage reactions are described for example in standard reference works, such as e.g., Science of Synthesis: Houben-Weyl Methods of Molecular Transformation. Georg Thieme Verlag, Stuttgart, Germany. 2005. 41627 pp. (URL: http://www.science-of-synthesis.com (Electronic Version, 48 Volumes)); J. F. W. McOmie, “Protective Groups in Organic Chemistry”, Plenum Press, London and New York 1973, in T. W. Greene and P. G. M. Wuts, “Protective Groups in Organic Synthesis”, Third edition, Wiley, New York 1999, in “The Peptides”; Volume 3 (editors: E. Gross and J. Meienhofer), Academic Press, London and New York 1981, in “Methoden der organischen Chemie” (Methods of Organic Chemistry), Houben Weyl, 4th edition, Volume 15/I, Georg Thieme Verlag, Stuttgart 1974, in H.-D. Jakubke and H. Jeschkeit, “Aminosäuren, Peptide, Proteine” (Amino acids, Peptides, Proteins), Verlag Chemie, Weinheim, Deerfield Beach, and Basel 1982, and in Jochen Lehmann, “Chemie der Kohlenhydrate: Monosaccharide and Derivate” (Chemistry of Carbohydrates: Monosaccharides and Derivatives), Georg Thieme Verlag, Stuttgart 1974. A characteristic of protecting groups is that they can be removed readily (i.e., without the occurrence of undesired secondary reactions) for example by solvolysis, reduction, photolysis or alternatively under physiological conditions (e.g., by enzymatic cleavage).

Acid addition salts of the compounds of the invention are most suitably formed from pharmaceutically acceptable acids, and include for example those formed with inorganic acids, e.g., hydrochloric, hydrobromic, sulphuric or phosphoric acids and organic acids, e.g., succinic, malaeic, acetic or fumaric acid. Other non-pharmaceutically acceptable salts, e.g., oxalates can be used for example in the isolation of the compounds of the invention, for laboratory use, or for subsequent conversion to a pharmaceutically acceptable acid addition salt. Also included within the scope of the invention are solvates and hydrates of the invention.

The conversion of a given compound salt to a desired compound salt is achieved by applying standard techniques, in which an aqueous solution of the given salt is treated with a solution of base e.g. sodium carbonate or potassium hydroxide, to liberate the free base which is then extracted into an appropriate solvent, such as ether. The free base is then separated from the aqueous portion, dried, and treated with the requisite acid to give the desired salt.

In vivo hydrolyzable esters or amides of certain compounds of the invention can be formed by treating those compounds having a free hydroxy or amino functionality with the acid chloride of the desired ester in the presence of a base in an inert solvent such as methylene chloride or chloroform. Suitable bases include triethylamine or pyridine. Conversely, compounds of the invention having a free carboxy group can be esterified using standard conditions which can include activation followed by treatment with the desired alcohol in the presence of a suitable base.

Mixtures of isomers obtainable according to the invention can be separated in a manner known per se into the individual isomers; diastereoisomers can be separated, for example, by partitioning between polyphasic solvent mixtures, recrystallisation or chromatographic separation, for example over silica gel or by, e.g., medium pressure liquid chromatography over a reversed phase column, and racemates can be separated, for example, by the formation of salts with optically pure salt-forming reagents and separation of the mixture of diastereoisomers so obtainable, for example by means of fractional crystallisation, or by chromatography over optically active column materials.

Intermediates and final products can be worked up or purified according to standard methods, e.g., using chromatographic methods, distribution methods, (re-) crystallization, and the like.

Methods of preparing decitabine are known in the art.

In another embodiment, the invention is directed to a method of coupling cyclic urea compounds such as imidazolidin-2-one, tetrahydropyrimidin-2(1H)-one, 1,3-diazepan-2-one or 1,3,4,7-tetrahydro-2H-1,3-diazepin-2-one (ER-878899) to a C-2-substituted tetrahydrofuran ring comprising forming a reaction mixture by mixing (i) a first solution comprising the 1,3,4,7-tetrahydro-2H-1,3-diazepin-2-one in a reaction solvent with (ii) a second solution comprising the C-2-substituted tetrahydrofuran ring in the reaction solvent under reflux conditions. In this embodiment, the reflux conditions can maintain the volume of the reaction mixture as the first solution is added to the second solution. Alternatively, the reflux conditions can prevent the volume of the reaction mixture from increasing by more than 50%, 40%, 30%, 20%, 10%, 5%, 4%, 3%, 2% or 1%. In this embodiment, the reaction solvent can be a polar, aprotic solvent having a boiling point greater than 150° C., such as dimethylacetamide (DMA) or dimethylsulfoxide (DMSO). According to this embodiment, the second solution is heated to greater than 150° C., and the first solution can be added via syringe to the second solution. According to this embodiment, the first solution can be added to the second solution over a time period extending less than 10 hours, less than 5 hours, less than 3 hours, less than 2 hours, less than 1 hour or less than 30 minutes. According to this embodiment, the second solution can be heated from 150° C. to 250° C., from 175° C. to 225° C., or from 200° C. to 220° C. According to this embodiment, the C-2-substituted tetrahydrofuran ring can have substituents in the C-3 position, which can include one halogen in the C-3 position, two halogens in the C-3 position, or two fluorines in the C-3 position. According to this embodiment, the tetrahydrofuran ring can be ER-878898. With the exception of mutually exclusive values, any of the alternative features described in this paragraph can be used together.

In another embodiment, the invention is directed to a method of isolating ER-879381 from a mixture comprising ER-878617 comprising (i) contacting the mixture with a chromatographic substance, and separating the mixture on the substance using toluene and acetonitrile as the mobile phase. According to this embodiment, the chromatographic substance can be silica gel. According to this embodiment, the mobile phase can be toulene:acetonitrile in a 7:1 ratio. Alternatively, according to this embodiment, the toulene:acetonitrile can have a ratio of greater than 7:1, or less than 7:1. With the exception of mutually exclusive values, any of the alternative features described in this paragraph can be used together.

Dosage Forms

In certain embodiments, the compositions of the instant invention (e.g., a compound of formula I in combination with dectabine, e.g., ER-876437 in combination with decitabine) can be administered to a subject in need thereof using the formulations and methods described in U.S. Pat. No. 7,144,873, U.S. Pat. No. 7,135,464, U.S. Pat. No. 6,982,253, U.S. Pat. No. 6,905,669, and U.S. Pat. No. 6,613,753, all of which are incorporated herein by reference in their entireties.

In some embodiments, pharmaceutical compositions of the compounds (or combinations) of the invention can be in unitary dosage form suitable for administration orally, rectally or by parenteral injection. For example, in preparing compositions in oral dosage form, any of the usual pharmaceutical media may be employed, such as, for example, water, glycols, oils, alcohols and the like, as in the case of oral liquid preparations such as suspensions, syrups, elixirs and solutions; or solid carriers such as starches, sugars, kaolin, lubricants, binders, disintegrating agents and the like in the case of powders, pills, capsules and tablets. Because of their ease in administration, tablets and capsules represent the most advantageous oral dosage unit form, in which case solid pharmaceutical carriers are employed. For parenteral compositions, carriers usually comprise sterile water, at least in large part, though other ingredients, for example, to aid solubility, may be included. Injectable solutions, for example, are prepared using a carrier which comprises saline solution, glucose solution or a mixture of saline and glucose solution. Injectable suspensions may also be prepared in which case appropriate liquid carriers, suspending agents and the like may be employed. In case of compositions suitable for percutaneous administration, carrier optionally comprises a penetration enhancing agent or a suitable wetting agent, which may be combined with suitable additives of any nature in minor proportions, which additives do not cause a significant deleterious effect to the skin. Additives may facilitate the administration to the skin or may be helpful for preparing desired compositions. These compositions may be administered in various ways, e.g., as a transdermal patch, as a spot-on, as an ointment.

It is especially advantageous to formulate the pharmaceutical compositions described herein in dosage unit form for ease of administration and uniformity of dosage. Dosage unit form, as used herein, refers to physically discrete units suitable as unitary dosages, each unit containing a predetermined quantity of active ingredient calculated to produce the desired therapeutic effect in association with the required pharmaceutical carrier. Examples of such dosage unit forms are tablets (including scored or coated tablets), capsules, pills, powder packets, wafers, injectable solutions or suspensions, teaspoonfuls, tablespoonfuls and the like, and segregated multiples thereof.

In general it is contemplated that a therapeutically effective amount of a first or a second compound would be from 0.0001 mg/kg to 0.001 mg/kg; 0.001 mg/kg to 10 mg/kg body weight or from 0.02 mg/kg to 5 mg/kg body weight. In some embodiments, a therapeutically effective amount of a first or a second compound is from 0.007 mg to 0.07 mg, 0.07 mg to 700 mg, or from 1.4 mg to 350 mg. A method of prophylactic or curative treatment may also include administering the composition in a regimen of between one to five intakes per day.

In some embodiments, a therapeutically effective amount of a first compound or a second compound includes, but is not limited to, the amount less than 0.01 mg/dose, or less than 0.5 mg/dose, or less than 1 mg/dose, or less than 2 mg/dose, or less than 5 mg/dose, or less than 10 mg/dose, or less than 20 mg/dose, or less than 25 mg/dose, or less than 50 mg/dose, or less than 100 mg/dose, or less than 500 mg/dose. The number of times a day a first or a second compound is administrated to a subject can be determined based on various criteria commonly used in the art or those described herein.

Wetting agents, emulsifiers and lubricants, such as sodium lauryl sulfate and magnesium stearate, as well as coloring agents, release agents, coating agents, sweetening, flavoring and perfuming agents, preservatives and antioxidants can also be present in the compositions.

Examples of pharmaceutically acceptable antioxidants include: water soluble antioxidants, such as ascorbic acid, cysteine hydrochloride, sodium bisulfate, sodium metabisulfite, sodium sulfite and the like; oil-soluble antioxidants, such as ascorbyl palmitate, butylated hydroxyanisole (BHA), butylated hydroxytoluene (BHT), lecithin, propyl gallate, α-tocopherol, and the like; and metal chelating agents, such as citric acid, ethylenediamine tetraacetic acid (EDTA), sorbitol, tartaric acid, phosphoric acid, and the like.

Formulations of the present invention include those suitable for oral, nasal, topical, buccal, sublingual, rectal, vaginal or parenteral administration. The formulations may conveniently be presented in unit dosage form and may be prepared by any methods well known in the art of pharmacy. The amount of active ingredient that can be combined with a carrier material to produce a single dosage form will generally be that amount of the composition that produces a therapeutic effect. Generally, out of one hundred percent, this amount will range from about 1 percent to about ninety-nine percent of active ingredient, preferably from about 5 percent to about 70 percent, most preferably from about 10 percent to about 30 percent.

Methods of preparing these formulations or compositions include the step of bringing into association a composition of the present invention with the carrier and, optionally, one or more accessory ingredients. In general, the formulations are prepared by uniformly and intimately bringing into association a composition of the present invention with liquid carriers, or finely divided solid carriers, or both, and then, if necessary, shaping the product.

Formulations of the invention suitable for oral administration may be in the form of capsules, cachets, pills, tablets, lozenges (using a flavored basis, usually sucrose and acacia or tragacanth), powders, granules, or as a solution or a suspension in an aqueous or non-aqueous liquid, or as an oil-in-water or water-in-oil liquid emulsion, or as an elixir or syrup, or as pastilles (using an inert base, such as gelatin and glycerin, or sucrose and acacia) or as mouth washes and the like, each containing a predetermined amount of a composition of the present invention as an active ingredient. A composition of the present invention may also be administered as a bolus, electuary or paste.

In solid dosage forms of the invention for oral administration (capsules, tablets, pills, dragees, powders, granules and the like), the active ingredient is mixed with one or more pharmaceutically acceptable carriers, such as sodium citrate or dicalcium phosphate, or any of the following: fillers or extenders, such as starches, lactose, sucrose, glucose, mannitol, or silicic acid; binders, such as, for example, carboxymethylcellulose, alginates, gelatin, polyvinyl pyrrolidone, sucrose or acacia; humectants, such as glycerol; disintegrating agents, such as agar-agar, calcium carbonate, potato or tapioca starch, alginic acid, certain silicates, and sodium carbonate; solution retarding agents, such as paraffin; absorption accelerators, such as quaternary ammonium compounds; wetting agents, such as, for example, cetyl alcohol and glycerol monostearate; absorbents, such as kaolin and bentonite clay; lubricants, such a talc, calcium stearate, magnesium stearate, solid polyethylene glycols, sodium lauryl sulfate, and mixtures thereof; and coloring agents. In the case of capsules, tablets and pills, the pharmaceutical compositions may also comprise buffering agents. Solid compositions of a similar type may also be employed as fillers in soft and hard-filled gelatin capsules using such excipients as lactose or milk sugars, as well as high molecular weight polyethylene glycols and the like.

A tablet may be made by compression or molding, optionally with one or more accessory ingredients. Compressed tablets may be prepared using binder (for example, gelatin or hydroxypropylmethyl cellulose), lubricant, inert diluent, preservative, disintegrant (for example, sodium starch glycolate or cross-linked sodium carboxymethyl cellulose), surface-active or dispersing agent. Molded tablets may be made by molding in a suitable machine a mixture of the powdered composition moistened with an inert liquid diluent.

The tablets, and other solid dosage forms of the pharmaceutical compositions of the present invention, such as dragees, capsules, pills and granules, may optionally be scored or prepared with coatings and shells, such as enteric coatings and other coatings well known in the pharmaceutical-formulating art. They may also be formulated so as to provide slow or controlled release of the active ingredient therein using, for example, hydroxypropylmethyl cellulose in varying proportions to provide the desired release profile, other polymer matrices, liposomes or microspheres. They may be sterilized by, for example, filtration through a bacteria-retaining filter, or by incorporating sterilizing agents in the form of sterile solid compositions that can be dissolved in sterile water, or some other sterile injectable medium immediately before use. These compositions may also optionally contain opacifying agents and may be of a composition that they release the active ingredient(s) only, or preferentially, in a certain portion of the gastrointestinal tract, optionally, in a delayed manner. Examples of embedding compositions that can be used include polymeric substances and waxes. The active ingredient can also be in micro-encapsulated form, if appropriate, with one or more of the above-described excipients.

Liquid dosage forms for oral administration of the compositions of the invention include pharmaceutically acceptable emulsions, microemulsions, solutions, suspensions, syrups and elixirs. In addition to the active ingredient, the liquid dosage forms may contain inert diluent commonly used in the art, such as, for example, water or other solvents, solubilizing agents and emulsifiers, such as ethyl alcohol, isopropyl alcohol, ethyl carbonate, ethyl acetate, benzyl alcohol, benzyl benzoate, propylene glycol, 1,3-butylene glycol, oils (in particular, cottonseed, groundnut, corn, germ, olive, castor and sesame oils), glycerol, tetrahydrofuryl alcohol, polyethylene glycols and fatty acid esters of sorbitan, and mixtures thereof.

Besides inert diluents, the oral compositions can also include adjuvants such as wetting agents, emulsifying and suspending agents, sweetening, flavoring, coloring, perfuming and preservative agents.

Suspensions, in addition to the active compositions, may contain suspending agents as, for example, ethoxylated isostearyl alcohols, polyoxyethylene sorbitol and sorbitan esters, microcrystalline cellulose, aluminum metahydroxide, bentonite, agar-agar and tragacanth, and mixtures thereof.

Formulations of the pharmaceutical compositions of the invention for rectal or vaginal administration may be presented as a suppository, which may be prepared by mixing one or more compositions of the invention with one or more suitable nonirritating excipients or carriers comprising, for example, cocoa butter, polyethylene glycol, a suppository wax or a salicylate, and which is solid at room temperature, but liquid at body temperature and, therefore, will melt in the rectum or vaginal cavity and release the active composition.

Formulations of the present invention which are suitable for vaginal administration also include pessaries, tampons, creams, gels, pastes, foams or spray formulations containing such carriers as are known in the art to be appropriate.

Dosage forms for the topical or transdermal administration of a composition of this invention include powders, sprays, ointments, pastes, creams, lotions, gels, solutions, patches and inhalants. The active composition may be mixed under sterile conditions with a pharmaceutically acceptable carrier, and with any preservatives, buffers, or propellants that may be required.

The ointments, pastes, creams and gels may contain, in addition to an active composition of this invention, excipients, such as animal and vegetable fats, oils, waxes, paraffins, starch, tragacanth, cellulose derivatives, polyethylene glycols, silicones, bentonites, silicic acid, talc and zinc oxide, or mixtures thereof.

Powders and sprays can contain, in addition to a composition of this invention, excipients such as lactose, talc, silicic acid, aluminum hydroxide, calcium silicates and polyamide powder, or mixtures of these substances. Sprays can additionally contain customary propellants, such as chlorofluorohydrocarbons and volatile unsubstituted hydrocarbons, such as butane and propane.

Transdermal patches have the added advantage of providing controlled delivery of a composition of the present invention to the body. Such dosage forms can be made by dissolving or dispersing the composition in the proper medium. Absorption enhancers can also be used to increase the flux of the composition across the skin. The rate of such flux can be controlled by either providing a rate controlling membrane or dispersing the active composition in a polymer matrix or gel.

Ophthalmic formulations, eye ointments, powders, solutions and the like, are also contemplated as being within the scope of this invention. Pharmaceutical compositions of this invention suitable for parenteral administration comprise one or more compositions of the invention in combination with one or more pharmaceutically acceptable sterile isotonic aqueous or nonaqueous solutions, dispersions, suspensions or emulsions, or sterile powders which may be reconstituted into sterile injectable solutions or dispersions just prior to use, which may contain antioxidants, buffers, bacteriostats, solutes which render the formulation isotonic with the blood of the intended recipient or suspending or thickening agents.

Examples of suitable aqueous and nonaqueous carriers that may be employed in the pharmaceutical compositions of the invention include water, ethanol, polyols (such as glycerol, propylene glycol, polyethylene glycol, and the like), and suitable mixtures thereof, vegetable oils, such as olive oil, and injectable organic esters, such as ethyl oleate. Proper fluidity can be maintained, for example, by the use of coating materials, such as lecithin, by the maintenance of the required particle size in the case of dispersions, and by the use of surfactants.

These compositions may also contain adjuvants such as preservatives, wetting agents, emulsifying agents and dispersing agents. Prevention of the action of microorganisms may be ensured by the inclusion of various antibacterial and antifungal agents, for example, paraben, chlorobutanol, phenol sorbic acid, and the like. It may also be desirable to include isotonic agents, such as sugars, sodium chloride, and the like into the compositions. In addition, prolonged absorption of the injectable pharmaceutical form may be brought about by the inclusion of agents that delay absorption such as aluminum monostearate and gelatin.

In some cases, in order to prolong the effect of a drug, it is desirable to slow the absorption of the drug from subcutaneous or intramuscular injection. This may be accomplished by the use of a liquid suspension of crystalline or amorphous material having poor water solubility. The rate of absorption of the drug then depends upon its rate of dissolution which, in turn, may depend upon crystal size and crystalline form. Alternatively, delayed absorption of a parenterally-administered drug form is accomplished by dissolving or suspending the drug in an oil vehicle.

Injectable depot forms are made by forming microencapsule matrices of the subject compositions in biodegradable polymers such as polylactide-polyglycolide. Depending on the ratio of drug to polymer, and the nature of the particular polymer employed, the rate of drug release can be controlled. Examples of other biodegradable polymers include poly(orthoesters) and poly(anhydrides). Depot injectable formulations are also prepared by entrapping the drug in liposomes or microemulsions that are compatible with body tissue.

The preparations of the present invention may be given orally, parenterally, topically, or rectally. They are of course given by forms suitable for each administration route. For example, they are administered in tablets or capsule form, by injection, inhalation, eye lotion, ointment, suppository, etc., administration by injection, infusion or inhalation; topical by lotion or ointment; and rectal by suppositories. Oral or 1V administration is preferred.

The phrases “parenteral administration” and “administered parenterally” as used herein means modes of administration other than enteral and topical administration, usually by injection, and includes, without limitation, intravenous, intramuscular, intraarterial, intrathecal, intracapsular, intraorbital, intracardiac, intradermal, intraperitoneal, transtracheal, subcutaneous, subcuticular, intraarticular, subcapsular, subarachnoid, intraspinal and intrasternal injection and infusion.

The phrases “systemic administration,” “administered systemically,” “peripheral administration” and “administered peripherally” as used herein mean the administration of a compound, drug or other material other than directly into the central nervous system, such that it enters the patient's system and, thus, is subject to metabolism and other like processes, for example, subcutaneous administration.

These compounds may be administered to humans and other animals for therapy by any suitable route of administration, including orally, nasally, as by, for example, a spray, rectally, intravaginally, parenterally, intracisternally and topically, as by powders, ointments or drops, including buccally and sublingually.

Regardless of the route of administration selected, the compounds of the present invention, which may be used in a suitable hydrated form, or the pharmaceutical compositions of the present invention, are formulated into pharmaceutically acceptable dosage forms by conventional methods.

Actual dosage levels of the active ingredients in the pharmaceutical compositions of this invention may be varied so as to obtain an amount of the active ingredient which is effective to achieve the desired therapeutic response for a particular patient, composition, and mode of administration, without being toxic to the patient.

The selected dosage level will depend upon a variety of factors including the activity of the particular compound of the present invention employed, or the ester, salt or amide thereof, the route of administration, the time of administration, the rate of excretion of the particular compound being employed, the duration of the treatment, other drugs, compounds or materials used in combination with the particular compound employed, the age, sex, weight, condition, general health and prior medical history of the patient being treated, and like factors well known in the medical arts.

A physician or veterinarian can determine and prescribe the effective amount of the pharmaceutical composition required. For example, the physician or veterinarian could start doses of the compounds of the invention employed in the pharmaceutical composition at levels lower than that required in order to achieve the desired therapeutic effect and gradually increase the dosage until the desired effect is achieved.

In general, a suitable daily dose of a compound of the invention will be that amount of the compound that is the lowest dose effective to produce a therapeutic effect. Such an effective dose will generally depend upon the factors described above. Generally, intravenous and subcutaneous doses of the compounds of this invention for a patient, when used for the indicated analgesic effects, will range from about 0.0001 to about 100 mg per kilogram of body weight per day, more preferably from about 0.01 to about 50 mg per kg per day, and still more preferably from about 1.0 to about 100 mg per kg per day. An effective amount is that amount treats a viral infection.

If desired, the effective daily dose of the active compound may be administered as two, three, four, five, six or more sub-doses administered separately at appropriate intervals throughout the day, optionally, in unit dosage forms.

While it is possible for a compound of the present invention to be administered alone, it is preferable to administer the compound as a pharmaceutical composition.

EXAMPLES

General methods and experimentals for preparing compounds of the present invention are set forth below.

Example I Chemical Syntheses

Unless otherwise stated, for Examples I.B.-I.C., solvent removal was carried out using a Büchi rotary evaporator. Analytical chromatography was carried out using a Hewlett Packard series 1100 HPLC and preparative chromatography was carried out using either Biotage SP4 instrument or a Waters 4000 instrument using Chiralpak IA columns under neutral condition, unless indicated otherwise. Mass spectra were recorded using Waters Acquity HPLC/MS system. Like or comparable equipment was used for the remaining examples.

NMR spectra were recorded using a Varian 400 MHz spectrometer (Examples I.B.-I.C.) or using a Fluka 400 MHz spectrometer (Examples I.A. and I.D.).

Example I.A. ER-876437 I.A.1: Preparation of ER-878899 (1,3,4,7-tetrahydro-2H-1,3-diazepin-2-one)

ER-878899 was prepared as outlined in Scheme I below. This preparation was described in J. Med. Chem. 1981, 24, 662-666; J. Org. Chem. 1980, 45, 485-489 and Bull. Soc. Chim. Fr. 1973, 198-292, all of which are hereby incorporated by reference in their entirety.

Mechanical stirring is required for the formation of ER-878899 made according to Scheme I. Carbonyl sulfide may be bubbled into the reaction flask using a glass pipette (of large diameter) and not a needle, which tends to clog due to the solid formed during the reaction. At the end of the reaction, the insoluble material in the reaction medium was filtered, and ER-878899 may be present in the filter cake.

I.A.2: Preparation of ER-876437

ER-878899, prepared according to I.A.1., was used in Scheme II as described below.

1-(3,3-Difluoro-4-benzoyl-5-benzoxymethyl-tetrahydro-furan-2-yl)-1,3,4,7-tetrahydro-[1,3]diazepin-2-one (ER-879381). The commercially available mesylate ER-878898 shown above in Scheme II (3.8 g, 8.3 mmol) and the urea ER-878899 (900 mg, 8.0 mmol) were added to dimethylacetamide (DMA) (400 ml). Upon heating (170° C.), the reaction components solubilized. The solution was heated overnight (15 h) under an atmosphere of nitrogen.

The DMA was then removed in vacuo. The residue was resuspended in EtOAc (150 ml) and then washed with water (2×75 ml). The combined organic layers were dried over MgSO₄, filtered, and concentrated in vacuo. The material was chromatographed on SiO₂ and was eluted with 50% EtOAc/hexanes. The material obtained after chromatography was the unresolved α/β anomers. The anomers were then separated using normal phase preparative HPLC (50% EtOAc/hexanes isocratic, 10 ml/min, Rt=25.7 min.); column: phenomenex luna 10μ Silica 100 A, 250×21.20 mm; refractive index detector. The β anomer ER-879381 was isolated in >90% purity (10% α anomer, Rt. 24 min). ¹H NMR (CDCl₃) δ 8.05 (m, 4H), 7.59 (m, 2H), 7.43 (m, 4H), 5.99 (m, 1H), 5.72 (m, 2H), 5.54 (m, 1H), 4.77 (dd, J=12.1, 3.4 Hz, 1H), 4.65 (br s, 1H), 4.56 (dd, J=12.4, 4.0 Hz, 1H), 4.38 (m, 1H), 3.80 (m, 4H).

1-(3,3-Difluoro-4-hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-1,3,4,7-tetrahydro-[1,3]diazepin-2-one (ER-876437). ER-879381 was dissolved in NH₃ (7M) in MeOH (40 ml). The solution stirred overnight. The solvent was removed and the residue was purified by RP HPLC (10% acetonitrile/H₂O, flow 10 ml/min, Rt=23 minutes); column: phenomenex luna 5μ C18(2) 100 A, 250×21.2 mm; refractive index detector. The desired compound ER-876437 was obtained in 1.5% (62 mg) overall yield. ¹H NMR (D₂O) δ 5.86 (m, 2H), 5.69 (dd, J=14.3 Hz, 6.2 Hz, 1H), 4.14 (m, 1H), 3.86 (m 1H), 3.74 (m, 6H). ¹³C NMR (D₂O) δ 164.5, 127.3, 126.2, 122.1 (dd, J=252, 261 Hz, 1C), 85.9 (dd, J=41, 22 Hz, 1C), 77.4 (d, J=8 Hz, 1C), 69.5 (dd, J=22 Hz, 19 Hz, 1C), 58.9, 41.0, 40.7.

The carbon, hydrogen and nitrogen components of the molecular formula (C₁₀H₁₄N₂O₄F₂+0.5H₂O) was calculated to be C, 43.96; H, 5.53; and N, 10.25. Elemental analysis revealed this material to contain C, 43.99; H, 5.36; and N, 10.21.

Marginal improvements to the yield of the coupling reaction of ER-878899 to the mesylate may be obtained by changing the reaction solvent. When diglyme is used as the solvent, a 15% yield improvement may be observed.

Example I.B. ER-876437 I.B.1: Preparation of ER-878899 (1,3,4,7-tetrahydro-2H-1,3-diazepin-2-one)

ER-878705 (shown below) was prepared following the procedure described in Feigenbaum, A. and Lehn, J. M., Bull. Soc. Chim. Fr., 1973, 198-202 and Liu, P. S., Marquez, V. E., Driscoll, J. S, and Fuller, R. W., J. Med. Chem., 1981, 24, 662-666.

To a white suspension of ER-878705 (79.7 g, 230 mmol) in ethanol (470 mL) in a two-neck 2 L flask equipped with mechanical stirrer was added hydrazine hydrate (23.5 mL, 483 mmol) at room temperature. The resulting white suspension was heated to 50° C. for 30 minutes to obtain a clear light yellow solution. As white precipitate started appearing, the mixture was heated to 60° C. for 3 hours and the stirring became very difficult. After allowing the mixture to cool to room temperature, concentrated hydrogen chloride solution (40.3 mL, 483 mmol) was added and the mixture became easily stirred. After stirring for 30 minutes, the mixture was filtered and washed with 5×200 mL of water. The filtrate was concentrated to a dry solid. The dry solid was suspended in 200 mL of ethanol, and stirred for 1 hour to make a nice suspension. The suspension was filtered and washed with 3×100 mL pure ethanol. The cake (white granular-like crystal) was collected and dried to give 34.6 (94%) g of 1,4-diamino-2-butene di-hydrochloride salt. ¹H NMR showed the product contains phthalhydrazide as a minor impurity in the ratio of 5:1. ¹H NMR (400 MHz, CD₃OD) δ 5.85 (ddd, J=1.6, 1.8 and 4.4 Hz, 2H), 3.69 (d, J=4.4, 4H).

To a suspension of 1,4-diamino-2-butene di-hydrochloride salt (22.7 g, 143 mmol) in ethanol (1.2 L) in a two-neck 2 L flask was added 1.0 M NaOH solution (330 mL, 330 mmol). Upon addition of NaOH to the suspension, the mixture became a transparent and colorless solution. The solution was heated to 70° C. and carbonyl sulfide was bubbled through the heated mixture. Thereafter, the mixture was heated to 80° C. at reflux. After 3 hours, the bubbling was stopped and the mixture was heated an additional 1.5 hours, cooled to room temperature and neutralized by addition of 1.0 N HCl (50 mmol). The mixture was concentrated to a dry gray solid. The solid was suspended in 1 L of methanol, stirred for 2 hours, filtered and washed with methanol. The filtrate was concentrated to about 200 mL volume, cooled to 0° C., filtered and washed with cold methanol. The solid was collected and dried to give 5.05 g product. ¹H NMR showed it contained very minor impurity phthalhydrazide in the ratio of 13:1. ¹H NMR (400 MHz, CD₃OD) δ 5.91 (ddd, J=0.8, 1.2 and 1.6 Hz, 2H), 3.67 (d, J=4.0, 4H). The mother liquor was concentrated to about 30 mL, cooled to −10° C., filtered and washed with cooled MeOH (−10° C.). The solid was collected and dried to give 7.10 g of product with minor contamination of phthalhydrazide in the ratio of 4:1 as determined by ¹H NMR.

I.B.2: Preparation of ER-878617

As depicted in Scheme V above, a solution of ER-878898 (1.33 g, 2.92 mmol, available from Waterstone or Depew Fine Chemical) and ER.-878899 (200.0 mg, 1.78 mmol) in dry DMA (30 mL) was heated and stirred at 180-190° C. (oil bath temperature) as DMA distilled out slowly. Additional azeotroped 1,3,4,7-tetrahydro-2H-1,3-diazepin-2-one (800.0 mg, 7.13 mmol) in DMA (50 mL) was added with syringe pump over 2 hours during this DMA distillation. After addition of all material, the reaction was kept at reflux for 30 minutes and allowed to cool down. The reaction mixture was concentrated in vacuo and the residue was purified with chromatography to give ER-878617 (624.8 mg, 45%) as a mixture of two epimers.

I.B.3: Preparation of ER-876437

As depicted in Scheme VI above, a solution of ER-878617 (624.8 mg, 1.32 mmol) in 7 M ammonia/methanol (53 mL) was stirred at ambient temperature for 18 hours. The reaction mixture was concentrated in vacuo and the residue was purified with preparative TLC to give a crude product (274.2 mg, 78%) as the mixture of two epimers. The mixture of two epimers were separated on preparative chromatography with Chiralpak IA column (Daicel Chemical Industries, Ltd., Tokyo Japan) to give ER-876437 (160.2 mg).

Example I.C. ER-876437 I.C.1: Preparation of ER-879381

ER-879381 was made according to Scheme VII as shown below. ER-878899 was prepared as described above in Example I.B.1.

As depicted in Scheme VII above, a solution of ER-878898 (8.0 g, 18 mmol, available from Waterstone or Depew Fine Chemical) and ER-878899 (1.2 g, 10.7 mmol) in dry DMA (100 mL) was heated and stirred at 200-220° C. (oil bath temperature) as DMA distilled out slowly. Additional azeotroped 1,3,4,7-tetrahydro-2H-1,3-diazepin-2-one (4.8 g, 42.9 mmol) in DMA (350 mL) was added through syringe pump over 2 hours during this DMA distillation. After addition of all material, the reaction was kept at reflux for 30 minutes and allowed to cool down. The reaction mixture was concentrated in vacuo and the residue was combined with the residue from a separate experiment conducted on the same scale using the same procedure. The combined residue was purified with silica gel chromatography (mobile phase: 50-100% AcOEt/Heptane) to give a mixture of two epimers (9.38 g). The mixture of two epimers was further separated with silica gel chromatography (mobile phase: toluene:acetonitrile=7:1) to produce ER-879381 (3.94 g).

I.C.2: Preparation of ER-876437

ER-876437 was prepared as shown below in Scheme VIII.

As depicted in Scheme VIII above, a solution of ER-879381 (3.8 g, 8.0 mmol) in 7 M ammonia/methanol (100 mL) was stirred at ambient temperature for 17 hours. The reaction mixture was concentrated in vacuo and the residue was purified with chromatography (mobile phase: 50-100% AcOEt/Heptane) to give ER-876437 (1.89 g, yield 89%).

Example I.D. ER-878895 I.D.1: Preparation of ER-878890

As depicted in Scheme IX above, a solution of ER-878889 (prepared according to Stimac, A. and Kobe, J., Carbohydr. Res., 2000, 329, 317-324, 4.3 g, 11.7 mmol) and di-tert-butyldicarbonate (5.4 g, 24.6 mmol) in THF (125 mL) was stirred in the presence of Lindlar's catalyst (1 g) at 30 psi over the weekend. The reaction suspension containing the hydrogenated product was filtered through Celite and concentrated. The residue was purified with radial chromatography to give ER-878890 (2.8 g). ER-878890 was further purified by recrystallization from AcOEt/Hexane to give white needles with mp 106-108° C.

I.D.2: Preparation of ER-878891

As depicted in Scheme X above, to a stirring solution of ER-878890 (1.6 g, 3.48 mmol) in THF/DMF (100 mL/30 mL) was added 0.5 M potassium hexamethyldisilazide (KHMDS) in toluene (8.5 mL, 4.25 mmol) dropwise at about −78° C. (dry ice/acetone bath), followed by addition of allyl bromide (0.4 mL, 4.6 mmol). The reaction mixture was stirred overnight as the dry ice-acetone bath slowly warmed to room temperature (˜25° C.). The reaction was quenched with saturated aqueous ammonium chloride and extracted with AcOEt. The organic phase was washed with brine and dried over anhydrous magnesium sulfate. The dried solution was filtered and evaporated. The residue was purified with radial chromatography to give ER-878891 (0.64 g).

I.D.3: Preparation of ER-878892

As depicted in Scheme XI above, to a stirring solution of ER-878891 (0.1 g, 0.2 mmol) in dichloromethane (DCM) (1 mL) under nitrogen was added trifluoroacetic acid (TFA) (0.5 mL) at room temperature. ER-878891 disappeared in 1 hour and the solvent and TFA were evaporated in vacuo. To the resulting oil redissolved in DCM (2 mL) was added allyl isocyanate (0.2 mL, 2.2 mmol) at room temperature. The reaction mixture was evaporated after 1 hour and purified by radial chromatography to give ER-878892 (50% yield) as a mixture of two anomers (beta/alpha ˜3/1).

I.D.4: Preparation of ER-878893

As depicted in Scheme XII above, to a stirring solution of ER-878892 (0.27 g, 0.56 mmol) in THF (10 mL) under nitrogen was added 0.5M KHMDS in toluene (1.5 mL, 0.75 mmol) at about −78° C. (dry ice/acetone bath), followed by addition of benzoyl chloride (0.6 mL, 5.1 mmol). The reaction mixture was stirred overnight and allowed to slowly warm to room temperature. The reaction was quenched with saturated aqueous ammonium chloride and extracted with AcOEt. The organic phase was washed with brine, dried over anhydrous magnesium sulfate, filtered and evaporated. The residue was purified with radial chromatography to give ER-878893 (0.13 g, 50% yield) as a mixture of anomers.

I.D.5: Preparation of ER-878894

As depicted in Scheme XIII above, to a degassed solution of ER-878893 (0.13 g, 0.22 mmol) in DCM (120 mL) was added Grubb's 2^(nd) generation catalyst (˜30 mg, available from Sigma-Aldrich, St. Louis, Mo.) under nitrogen. This catalyst affords the ring closing metathesis (RCM). The reaction mixture was heated at 40° C. for 1 hour followed by evaporation of the solvent. To the residue dissolved in AcOEt (20 mL) was added Silicycle Si-triamine Pd scavenger (Silicycle Inc.) and stirred vigorously for 1 hour. The reaction mixture was filtered and concentrated. The resulting pale yellow viscous oil was purified with radial chromatography and the less polar compound was determined to be ER-878894 (40 mg) which crystallized on standing.

I.D.6: Preparation of ER-878895

As depicted in Scheme XIV above, a solution of ER-878894 (65 mg, 0.14 mmol) in 0.1N NaOH/MeOH (3 mL) was stirred for 30 minutes until all of the UV active spots disappeared by TLC. The solvent was removed in vacuo and the crude solid was dissolved in water (2 mL). The solution was neutralized with HCl and the solvent was removed in vacuo. The residue was purified by reverse phase preparative HPLC to afford ER-878895 (12 mg, 35%).

Table 1 provides analytical data for compounds described herein.

TABLE 1 Analytical Data Structure ER-# Analytical Data

878617 Salt free ¹H NMR: (400 MHz, CDCl₃) δ 8.05 (m, 4H), 7.55 (m, 2H), 7.45 (m, 4H), 6.22 (t, J = 10.4 Hz), 5.95 (dd, J = 12.8, 10.6 Hz), 5.88-5.66 (m), 5.5 (m), 4.76 (dd, J = 12.4, 3.6 Hz), 4.65 (m), 4.55 (m), 4.55 (dd, J = 12, 4.4 Hz), 4.36 (m), 3.94-3.64 (m) MS (ESI) m/z 473.31 (M + H)⁺

879381 Salt free ¹H NMR: (400 MHz, CDCl₃) δ 8.05 (m, 4H), 7.64 (m, 2H), 7.48 (m, 4H), 6.04 (dd, J = 12.0, 10.4 Hz, 1H), 5.76 (m, 2H), 5.58 (ddd, J = 12.0, 6.4, 5.2 Hz, 1H), 4.81 (dd, J = 12.4, 3.6 Hz, 1H), 4.61 (dd, J = 12.8, 4.4 Hz, 1H), 4.58 (broad, partially overlap with 4.61 peaks, 1H), 4.43 (dt, J = 6.4, 3.4 Hz, 1H), 3.99-3.71 (m, 4H)

876437 Salt free ¹H NMR: (400 MHz, CD₃OD) δ 5.83 (m, 2H), 5.69 (dd, J = 21.2, 8.0 Hz, 1H), 4.05 (ddd, J = 14.0, 11.2, 8.4 Hz, 1H), 3.86- 3.58 (m, 7H) MS (ESI) m/z 265.17 (M + H)⁺

878890 Salt free ¹H NMR: (400 MHz, CDCl₃) δ 8.11-8.00 (m, 4H), 7.66-7.53 (m, 2H), 7.52-7.40 (m, 4H), 5.86 (dd, J = 16, 10 Hz, 1H), 5.57 (d, J = 18 Hz, 1H), 5.41 (s, 1H), 5.30 (s, 1H), 5.23 (d, J = 50 Hz, 1H), 4.60 (s, 2H), 1.47 (s, 9H)

878891 Salt free ¹H NMR: (400 MHz, CDCl₃) δ 8.08 (d, J = 7.6 Hz, 2H), 8.05 (d, J = 8.0 Hz, 2H), 7.62 (t, J = 7.6 Hz, 1H), 7.56 (t, J = 7.6 Hz, 1H), 7.46 (m, 4H), 6.0 (dd, J = 18.4, 4.4 Hz, 1H), 5.88 (m, 1H), 5.71 (dt, J = 19.6, 3.2 Hz, 1H), 5.48 (d, J = 52 Hz, 1H), 5.18 (d, J = 17.2 Hz, 1H), 5.14 (d, J = 10.8 Hz, 1H), 4.61 (broad s, 3H), 3.93 (m, 2H), 1.47 (s, 9H)

878892 Salt free ¹H NMR: (400 MHz, CDCl₃) δ 8.11- 8.00 (m, 4H), 7.66-7.53 (m, 2H), 7.52- 7.40 (m, 4H), 6.35 (dd, J = 26, 3 Hz, 1H), 6.06 (dd, J = 18, 5 Hz, 1H), 6.00-5.79 (m, 3H), 5.67 (dt, J = 19, 4 Hz, 1H), 5.58-5.50 (m, 1H), 5.44-4.95 (m, 8H), 4.74-4.53 (m, 4H), 4.01-3.97 (m, 2H), 3.91-3.83 (m, 3H), 1.71 (s, 1H)

878894 Salt free ¹H NMR: (400 MHz, CDCl₃) δ 8.12 (dd, J = 8.2, 1.2 Hz, 2H), 7.98 (dd, J = 8.2, 1.2 Hz, 2H), 7.6 (m, 5H), 7.45, (m, 6H), 5.93 (dd, J = 24.4, 3 Hz, 1H), 5.79 (s, 2H), 5.59 (dd, J = 18.6, 3.2 Hz, 1H), 5.14 (dd, J = 50.8, 2.8 Hz, 1H), 4.85 (d, J = 18.8 Hz, 1H), 4.81 (dd, J = 12, 3.8 Hz, 1H), 4.72 (dd. J = 12, 4.8 Hz, 1H), 4.35 (m, 2H), 4.17 (m, 2H) MS (ESI) m/z 559.2 (M + H)⁺

878895 Salt free ¹H NMR: (400 MHz, D₂O) δ 5.8 (m, 2H), 5.7 (dd, J = 18.4, 5.2 Hz, 1H), 4.93 (ddd, J = 53, 5.2, 3.8 Hz, 1H), 4.19 (ddd, J = 22.8, 6.4, 3.6 Hz, 1H), 3.84-3.61 (m, 7H) MS (ESI) m/z 247.11 (M + H)⁺

Example II Assay for Inhibition of Cytidine Deaminase (CDA)

The cytidine deaminase (CDA) enzymatic assay described by Cacciamani, T. et al., Arch. Biochem. Biophys. 1991, 290, 285-92; Cohen R. et al., J. Biol. Chem., 1971, 246, 7566-8; and Vincenzetti S. et al., Protein Expr. Purif 1996, 8, 247-53 was used to determine the inhibitory activity (IC₅₀) of compounds described herein. Using this assay, the IC₅₀ of these compounds was determined by following the decrease of substrate (cytidine) caused by the deamination reaction catalyzed by CDA. Disappearance of substrate (cytidine) over time was monitored by the absorbance at 280 nm of the reaction.

The assay reaction was carried out in potassium phosphate buffer (pH 7.4, 20 mM, containing 1 mM DTT) in a total volume of 100 μl in a 96-well plate format. The final reaction mixture contained cytidine (50 μM) and purified human recombinant CDA. Purified enzyme was diluted so as to produce an absorbance change of approximately 2 milli-absorbance units/minute. Base line measurements of absorbance change over time were made before substrate (cytidine) addition. After substrate addition, absorbance change was read every minute for 30 minutes with a FlexStation® 3 (Molecular Devices, Sunnyvale, Calif.). For each compound, 8 different concentrations (10 μM, 3.33 μM, 1.11 μM, 0.37 μM, 0.12 μM, 0.041 μM, and 0.014 μM, and 0.0047 μM) were used to inhibit the reaction. The slopes of the absorbance change over time in each reaction were calculated and used by the SoftMax® Pro 5 software (Molecular Devices, Sunnyvale, Calif.) to obtain IC₅₀ values.

TABLE 2 Inhibitory Potency of Test Compounds Structure ER-Number IC₅₀ (nM)

876437 237 ± 86 n = 4

876400 101 ± 53 n = 4

878519 1616 ± 643 n = 3

878895 140 n = 1

876404 113 n = 2

Example III Pharmacokinetics of ER-876437 and ER-876400 in Mice after IV and PO Administrations

ER-876437 and ER-876400 were both administered to mice at 10 mg/kg intravenously (IV) via the tail vein, and at 10 mg/kg per os (PO, or, orally) via gastric gavage. All doses were prepared in phosphate buffered saline (PBS) and were administered at a volume of 5 mL/kg. Five mice per group were used in these studies. Blood samples were taken serially from the tail vein of each mouse at predetermined timepoints. Blood samples from all mice in each group were pooled together prior to processing for plasma. The pooled blood samples were spun down within 30-60 minutes after withdrawal and the plasma was harvested and frozen for assay. After preparation and extraction the samples were assayed by LC/MS/MS. The observed concentrations (ng/mL), are reported in Table 3 below.

TABLE 3 Plasma concentrations (ng/mL) of ER-876437 and ER- 876400 in mice after IV and PO administrations ER-876437 ER-876400 Time (hr) IV PO IV PO 0.167 11838 8597 19860 7101 0.5 7686 3720 10166 7859 1 3469 4179  4206 4665 2 1450 1145    1753 ^(a) 1750 4 214 146     495 ^(a) 320 6 184 36  118 87 8 64 103   59 44 24 20 39   93 264 ^(a) Above the quantitation limit

The pharmacokinetic (PK) parameters of ER-876437 and ER-876400 were calculated via non-compartmental analysis using Watson® v. 7.2. The resulting PK parameters are presented in Tables 4 and 5 below:

TABLE 4 PK parameters of ER-876437 and ER-876400 in mice after IV administrations Parameter Units ER-876437 ER-876400 Dose mg/kg 10.0 10.0 t_(1/2) hr 6.1 16.1 AUC_(0-t) ng · hr/mL 12893 18838 AUC_(0-∞) ng · hr/mL 13071 20999 AUC_(0-∞)/D ng · hr/mL/D 1307 2100 AUC_(Extrap) % 1.4 10.3 CL L/kg/hr 0.77 0.48 Vss L/kg 1.64 3.2

TABLE 5 PK parameters of ER-876437 and ER-876400 in mice after PO administrations Parameter Units ER-876437 ER-876400 Dose mg/kg    10.0 10.0 C_(max) ng/mL 8597 7859 t_(max) hr     0.167 0.5 AUC_(0-t) ng · hr/mL 8579 13160 AUC_(0-∞) ng · hr/mL 9499 NC AUC_(0-∞)/D ng · hr/mL/D  950 NC AUC_(Extrap) %    9.7 NC t_(1/2) hr    16.3 NC F %    66.5 ^(a) 69.9 ^(a) ^(a) Calculated based on AUC_(0-t) NC = Not calculated due to insufficient data

The results of the present study suggest that the PK profiles of ER-876437 and ER-876400 in male BALB-c mice are similar. Following 10 mg/kg IV the PK of both ER-876437 and ER-876400 can be characterized by moderate distribution (Vss=1.64 and 3.20 L/kg, respectively), slow clearance (CL=0.77 and 0.48 L/hr/kg, respectively), and slow elimination (t_(1/2)=6.1 and 16.1 hr, respectively).

The overall exposures (AUC_(0-∞)) after IV administration of ER-876437 and ER-876400 to mice were 13071 and 20999 ng·hr/mL, respectively, which resulted in dose-normalized exposures (AUC_(0-∞)/D) of respectively 1307 and 2100 mL/g. Following 10 mg/kg PO, the C_(max) of ER-876437 and ER-876400 were respectively 8597 and 7859 ng/mL, and were observed at a t_(max) of respectively 1.0 and 2.0 hr. The AUC_(0-t) after PO administration of 10 mg/kg were 8579 and 13160 ng·hr/mL for ER-876437 and ER-876400, respectively. The AUC_(0-∞) of ER-876437 was 9499 ng·hr/mL and the t_(1/2) was 16.3 hr. Due to insufficient data in the terminal elimination phase these parameters could not be determined for ER-876400. In addition, the t_(1/2) for ER-876437 after PO administration is roughly 2.5-fold higher that that after IV administration.

The bioavailabilities (F %) of ER-876437 and ER-876400 were similar: 66.5 and 69.9%, respectively.

In conclusion, the PK profiles of ER-876437 and ER-876400 in male BALB-c mice after a single IV or PO dose of 10 mg/kg are similar. It is noted, however, that under normal feeding conditions, mice have a high gastric pH of around 5. See Simpson, R. J. et al. “Forms of soluble iron in mouse stomach and duodenal lumen: significance for mucosal update,” British Journal of Nutrition. 63:79-89 (1990), which is hereby wholly incorporated by reference.

Example IV ER-876400 and ER-876437 Stability in Simulated Gastric Fluid at 37° C.

This example describes the stabilities of ER-876400 and ER-876437 in simulated gastric fluid having a pH of 1.45 at room temperature (˜25° C.) and at 37° C. For humans, under fasted conditions, the gastric pH has been reported to range from 1.4 to 2.1. See Kararli, T. T. Comparison of the GI anatomy, physiology, and biochemistry of humans and commonly used laboratory animals. Bio Pharm & Drug Dispos. 16:351-380, 1995, which is hereby wholly incorporated by reference. The gastric pH in fasted monkeys has been reported to have a similar range of 1-3. See Kondo, H. et al. Characteristics of the gastric pH profiles of unfed and fed cynomolgus monkeys as pharmaceutical product development subjects. Bio Pharm & Drug Dispos. 24:45-51, 2003, which is hereby wholly incorporated by reference.

Materials: Simulated gastric fluid (SGF) was prepared by mixing the following into 100 mL of HPLC grade (or purified) water: 200 mg of sodium chloride and 1.87 mL of a 37.52% HCl stock solution.

Sample Preparation: The initial (t=0) samples were prepared by respectively diluting ER-876400 or ER-876437 in water. All other samples were prepared by dissolving ˜2 mg of analyte (either ER-876400 or ER-876437) in ˜1.0 mL of simulated gastric fluid at 37° C.

The HPLC analyses were conducted using a Waters HPLC solvent delivery system with Corona CAD detection. The HPLC Column (Waters Atlantis HHS T3 2.1×100 mm, 1.8 um) was maintained at 40° C. and preequilibrated with a solution containing 98% water and 2% acetonitrile. The temperature controlled auto-sampler was maintained at 37° C. The flow rate for the Water/MeCN mobile phase was 0.65 mL/min, with a gradient following sample injection (5 μL) as follows:

Gradient: Time (min) % Water % MeCN 0-2 98 2   2-2.5 linear gradient from (98% Water/2% MeCN) to (60% Water/40% MeCN) 2.5-3.5 60 40

Hence, in these HPLC-SGF degradation studies, a 5 μL aliquot was taken from the SGF/analyte solution at various times and loaded onto the HPLC column with the above described features and conditions. The Water/MeCN mobile phase was applied to the column with the above described flow rate and gradient and the HPLC chromatograms were collected. After 3.5 minutes, the column was reequilibrated with 98% water/2% MeCN for 1.5 minutes.

HPLC chromatograms of either ER-876400 or ER-876437 in water afforded identification of the peak attributed to ER-876400 or ER-876437. HPLC traces of SGF without any ER-876400 or ER-876437 provided blank (or background) chromatograms that could be used to identify SGF-related peaks and to distinguish those peaks from the analytes' peaks. Chromatograms were collected at the times identified in Tables 6 and 7, and the corresponding percentage of sample respectively attributed to either ER-876400 or ER-876437 are provide for each sampling time. These results are also depicted as plots in FIGS. 1 and 2.

TABLE 6 Stability of ER-876400 in SGF at 37° C. % ER-876400 Analysis Time (peak retention (hours:minutes:seconds) time: 1.46 min) 0:00:00 84.04 0:00:30 19.59 0:06:08 17.04 0:11:45 16.72 0:17:23 15.17 0:23:01 14.20 0:28:38 13.23 0:34:16 12.51 0:39:54 14.05 0:45:33 11.42 0:51:10 10.71 0:56:48 8.87 1:02:27 9.14 1:08:07 8.81 1:13:46 7.66 1:19:23 4.05 1:25:01 6.44 1:30:38 5.92 1:36:16 5.72 1:41:53 5.69 1:47:32 4.98 1:53:10 4.51 1:58:49 3.85 2:04:28 3.59 2:21:24 2.82 2:49:37 1.52 3:17:48 0.81 3:23:28 0.62 3:46:00 0.39 3:51:38 0.25

TABLE 7 Stability of ER-876437 in SGF at 37° C. % ER-876437 Analysis Time (peak retention (Hours:Minutes:Seconds) time: 2.90 min) 0:00:00 92.18 0:00:30 85.88 0:06:08 85.72 0:11:45 86.46 0:17:24 86.38 0:23:02 83.22 0:28:39 83.48 0:34:17 83.80 0:39:54 84.16 0:45:32 82.62 0:51:10 82.41 0:56:47 82.45 1:02:26 82.45 1:08:04 82.55 1:13:41 83.11 1:19:19 81.82 1:24:56 81.24 1:30:33 79.20 1:36:10 79.14 1:41:47 78.47 1:47:24 77.88 1:53:02 78.29 1:58:39 78.56 2:04:16 77.21 2:21:12 76.06 2:26:50 77.34 2:49:21 75.34 3:17:30 72.37 3:51:16 50.13 4:19:26 51.88 4:47:38 48.95 5:21:25 45.19 5:49:35 47.44 6:17:45 44.94 6:51:31 43.29 7:19:40 41.85 7:47:22 41.72 8:21:11 36.89 8:49:19 37.52 9:17:30 36.34 9:51:17 34.61 10:19:29  31.94 10:47:39  32.33 11:15:53  29.85 11:49:44  29.94 12:17:54  27.99 12:46:10  27.39 13:20:01  26.14

Conclusion: In simulated gastric fluid at 37° C., ER-876400 was found to degrade by 50% in less than 30 seconds while ER-876437 has a half-life of roughly 4-6 hours.

Example V Effect of ER-876437 on Decitabine in Survival Murine Lymphoma L1210 Model

The purpose of this study was to determine if ER-876437 enhances the oral efficacy of decitabine in the L1210 survival model in mice.

Preparation of L1210 Cells: L1210 ascitic cells were prepared by passaging them in mice at least three times as follows. Each CD2F1 female mouse was intraperitoneally (IP) injected with about 10⁵ L1210 ascitic cells. After one week, the mouse was sacrificed (asphyxiation via CO₂). The mouse was placed on its back, its belly surface was cleaned with alcohol wipes, and a small incision was made into the peritoneal cavity. 2 ml of ice cold 2.1% BSA in saline was injected into the cavity and then the fluid was withdrawn and transferred with an 18G 3 cc syringe into a clean sterile tube and kept on ice. The fluid was diluted 1:10 in 2.1% BSA in saline and one drop of Zap o globin II lytic reagent (available from Beckman Coulter, Inc.) was added to 1 ml of diluted ascites. Diluted ascites (diluted 1:10 again) were counted on a hematocytometer and the number of cells per mL was calculated. About 10⁵ L1210 cells were used for a subsequent passage for another mouse passage. Or, a stock of L1210 ascites in BSA solution was diluted to 1×10⁴ cells/0.1 ml for use in the study mice.

Preparation of Study Mice: 35 CD2F1 6-7 weeks old female mice were randomly separated into the 7 groups identified in Table 8. The mice were prepared with intravenous (IV) injection of L1210 ascites (prepared as described above) one day prior to commencing the dosing. Mice were injected with 0.1 ml of cell solution via caudal vein with a 27G needle. The total IV injection for all mice took about 50 minutes.

Mice were dosed with vehicle or ER-876437 per os (PO, i.e., orally) 30 minutes prior to dosing with decitabine. ER-876437 was prepared at 1 mg/ml in PBS and then diluted to 0.1 mg/ml and 0.01 mg/ml in PBS for the lower doses.

Decitabine was prepared at a 1 mg/ml stock in PBS and appropriately diluted to achieve a 0.01 mg/ml dosing solution. ER-876437 was prepared at the beginning of each day of dosing and stored at 4° C. Decitabine was prepared fresh twice a day, just prior to dosing. All solutions were stored on ice while dosing. Mice were dosed (intraperitoneally (IP) or per os (orally, PO)) twice a day (8 hours apart) for 4 consecutive days. Final dosing scheme and total decitabine and ER-876437 dose is outlined in Table 8.

TABLE 8 Dosing Scheme decitabine Cumulative Dose Cumulative ER-876437 ER-876437 Group # Drug (rte Adm) decitabine Dose Dose Dose 1 Vehicle Veh   0 mg/kg Veh 0 mg/kg 2 ER-876437 Veh   0 mg/kg 10 mg/kg 80 mg/kg  3 decitabine 0.1 mg/kg 0.8 mg/kg Veh 0 mg/kg PO 4 decitabine/ER- 0.1 mg/kg 0.8 mg/kg 0.1 mg/kg  0.8 mg/kg   876437 PO 5 decitabine/ER- 0.1 mg/kg 0.8 mg/kg  1 mg/kg 8 mg/kg 876437 PO 6 decitabine/ER- 0.1 mg/kg 0.8 mg/kg 10 mg/kg 80 mg/kg  876437 PO 7 decitabine 0.1 mg/kg IP 0.8 mg/kg Veh 0 mg/kg

Survival and Autopsy: Mice were observed for survival and weighed daily (Mon-Fri) for the duration of the study (30 days). Dead mice were autopsied and observed for the presence of tumors in organs. Tumor deaths were determined by liver weights greater than 1.6 g and spleen weights greater than 150 mg as per Covey J M and Zaharko D S, Eur J Cancer Clin Oncol, Vol. 21 p. 109-117, 1985.

Results:

Mice dosed with decitabine and decitabine plus ER-876437 lived longer than vehicle controls and ER-876437 alone (Table 9 and 10; p<0.05). No dose response was observed with ER-876437 in combination with decitabine.

0.1 mg/kg decitabine PO was slightly less effective than 0.1 mg/kg decitabine IP (Tables 9 and 10; p=0.0047). Co-administration of ER-876437 with 0.1 mg/kg decitabine regardless of ER-876437 dose significantly enhanced survival (days) compared to 0.1 mg/kg decitabine PO or IP (Tables 9 and 10; p<0.05), but there was no dose response between ER-876437 doses.

Table 9 lists the mean survival of each treatment group and the percent ILS (increased life span) compared to the vehicle group. All treated groups lived significantly longer than vehicle controls and CDA inhibitor alone groups (p<0.05).

Listed in Table 9 are the weight of the livers and spleens of mice on autopsy. All mice died a ‘tumor burden’ related death as indicated by the liver weights greater than 1.6 gram and the spleen weights greater than 150 mg (Covey et al Eur J Cancer Oncol 1985).

Gross observations were noted concerning the overall appearance of the peritoneal and thoracic cavities; however, there were no formal analysis of these observations.

TABLE 9 Effect of decitabine and ER-876437 on survival and liver and spleen weights in the L1210 IV Survival Model Mean % ILS Survival (Increased Mean Liver Mean Spleen Group (days) ± SD Life Span) wts (g) ± SD wts (g) ± SD Veh/veh  7.4 ± 0.55 1.79 ± 0.34 0.35 ± 0.03 Veh/decitabine 0.1 mg/kg PO 11.2 ± 0.45 51.35 2.17 ± 0.1  0.34 ± 0.04 Veh/decitabine 0.1 mg/kg IP 13.4 ± 0.89 81.08 1.81 ± 0.25 0.37 ± 0.14 ER-876437 0.1 mg/kg/decitabine 15.8 ± 1.48 113.51 1.92 ± 0.16 0.24 ± 0.04 0.1 mg/kg PO ER-876437 1 mg/kg/decitabine 16.6 ± 1.52 124.32  2.2 ± 0.46 0.28 ± 0.13 0.1 mg/kg PO ER-876437 10 mg/kg/decitabine 17.2 ± 2.39 132.43 2.18 ± 0.31 0.38 ± 0.12 0.1 mg/kg PO ER-876437 10 mg/kg/Veh  7.6 ± 0.89 2.70 2.02 ± 0.07 0.37 ± 0.04 ${*\%\mspace{14mu}{ILS}} = {\frac{\begin{matrix} {{{mean}\mspace{14mu}{survival}\mspace{14mu}{of}\mspace{14mu}{experimental}\mspace{14mu}({days})} -} \\ {{mean}\mspace{14mu}{survival}\mspace{14mu}{controls}\mspace{14mu}({days})} \end{matrix}}{{Mean}\mspace{14mu}{survival}\mspace{14mu}{of}\mspace{14mu}{control}\mspace{14mu}({days})} \times 100}$

TABLE 10 Statistical Analysis (Log Rank Test as per Prism GraphPad) Comparison P value Control vs 0.1 mg/kg decitabine PO 0.0023 Control vs 0.1 mg/kg decitabine IP 0.0023 Control vs ER-876437 alone 0.601 decitabine 0.1 mg/kg PO vs. decitabine 0.1 mg/kg IP 0.0047 Control vs ER-876437 0.1 mg/kg/decitabine 0.1 mg/kg PO 0.0023 decitabine 0.1 mg/kg PO vs. ER-876437 0.1 mg/kg/ 0.0016 decitabine 0.1 mg/kg PO decitabine 0.1 mg/kg PO vs. ER-876437 1 mg/kg/ 0.0016 decitabine 0.1 mg/kg PO decitabine 0.1 mg/kg PO vs. ER-876437 10 mg/kg/ 0.0016 decitabine 0.1 mg/kg PO decitabine 0.1 mg/kg IP vs. ER-876437 0.1 mg/kg/ 0.0119 decitabine 0.1 mg/kg PO decitabine 0.1 mg/kg IP vs. ER-876437 1 mg/kg/ 0.0034 decitabine 0.1 mg/kg PO decitabine 0.1 mg/kg IP vs. ER-876437 10 mg/kg/ 0.0034 decitabine 0.1 mg/kg PO ER-876437 0.1 mg/kg/decitabine 0.1 mg/kg PO vs. 0.4069 ER-876437 1 mg/kg/decitabine 0.1 mg/kg PO ER-876437 1 mg/kg/decitabine 1 mg/kg PO vs. 0.6131 ER-876437 10 mg/kg/decitabine 0.1 mg/kg PO Conclusion:

Decitabine plus ER-876437 was more efficacious in the L1210 IV survival model than decitabine alone regardless of the route administration of decitabine (PO or IP). There was no dose response between 0.1 mg/kg, 1 mgkg and 10 mg/kg of ER-876437 plus decitabine groups. This experiment was repeated in Example VI but using lower doses of ER-876437 to determine the minimally effective dose.

Example VI Effect of ER-876437 on Decitabine in Survival Murine Lymphoma L1210 Model

This example followed all the methods and protocols of Example V with the following changes: 40 CD2F1 6-7 weeks old female mice were randomly separated into the 8 groups identified in Table 11. Preparation of study mice with IV injection of L1210 ascites took about 60 minutes. ER-876437 was prepared at 1 mg/ml in PBS and then diluted to 0.1 mg/ml, 0.01 mg/ml and 0.001 mg/ml in PBS. All solutions were stored on ice while dosing. Mice were dosed (IP or PO) twice a day (7 or 8 hours apart) for 4 consecutive days.

TABLE 11 Dosing Scheme Decitabine Cumulative ER- ER- Dose Decitabine 876437 876437 Group # Drug (rte Adm) Dose Dose Dose 1 Vehicle Vehicle   0 mg/kg Vehicle 0 mg/kg 2 ER-876437 Vehicle   0 mg/kg 1 mg/kg 8 mg/kg 3 decitabine 0.1 mg/kg PO 0.8 mg/kg Veh 0 mg/kg 4 decitabine/ER- 0.1 mg/kg PO 0.8 mg/kg 0.01 mg/kg   0.08 mg/kg   876437 5 decitabine/ER- 0.1 mg/kg PO 0.8 mg/kg 0.1 mg/kg   0.8 mg/kg   876437 6 decitabine/ER- 0.1 mg/kg PO 0.8 mg/kg 1 mg/kg 8 mg/kg 876437 7 decitabine 0.1 mg/kg IP 0.8 mg/kg Vehicle 0 mg/kg  8* decitabine 0.1 mg/kg PO 0.8 mg/kg Vehicle 0 * Dosed twice a day, 8 hours apart. All other groups were dosed twice a day, 7 hours apart. Results:

Mice dosed with decitabine and decitabine plus ER-876437 lived longer than vehicle controls and ER-876437 alone (Tables 12 and 13; p<0.05). There was no difference in survival of mice dosed with 0.1 mg/kg decitabine PO when dosed 7 or 8 hours apart (Tables 12 and 13).

0.1 mg/kg decitabine PO was less effective than 0.1 mg/kg decitabine IP (Tables 12 and 13; p=0.0086). Co-administration of 0.01 mg/kg ER-876437 with 0.1 mg/kg decitabine PO had no effect on extending survival in L1210 leukemic mice compared to decitabine PO alone. Co-administration of 0.1 mg/kg and 1 mg/kg ER-876437 with 0.1 mg/kg decitabine PO significantly enhanced survival (days) compared to 0.1 mg/kg decitabine PO alone. Co-administration of 0.1 mg/kg and 1 mg/kg with 0.1 mg/kg decitabine PO alone was not statistically different than 0.1 mg/kg decitabine administered via IP. ER-876437 had a slight dose response at these low doses: 0.01 mg/kg was ineffective at enhancing the effect of decitabine delivered orally while both 0.1 mg/kg and 1 mg/kg significantly enhanced survival (p=0.04 and p=0.005 respectively; Table 13). The two higher doses of ER-876437 in combination with decitabine PO had a slight dose response (p=0.09; Table 13).

Table 12 lists the mean survival of each treatment group and the percent ILS (increased life span) compared to the vehicle group. All treated groups live significantly longer than vehicle controls and groups given ER-876437 only (p<0.05).

Listed in Table 12 are the weight of the livers and spleens of mice on autopsy. All mice died a ‘tumor burden’ related death as indicated by the liver weights greater than 1.6 gram and the spleen weights greater than 150 mg (Covey J M and Zaharko D S, Eur J Cancer Clin Oncol, Vol. 21 p. 109-117, 1985).

Gross observations were noted concerning the overall appearance of the peritoneal and thoracic cavities; however, there were no formal analysis of these observations.

TABLE 12 Effect of Decitabine and ER-876437 on survival and liver and spleen weights in the L1210 IV Survival Model Mean % ILS Survival (Increased Mean Liver Mean Spleen Group (days) ± SD Life Span) wts (g) ± SD wts (g) ± SD Veh/Veh   8 ± 0.71 1.95 ± 0.15 0.35 ± 0.03 Veh/decitabine 0.1 mg/kg PO 11.8 ± 0.84 47.50 2.02 ± 0.31 0.36 ± 0.11 Veh/decitabine 0.1 mg/kg PO (8 hr.) 11.6 ± 0.55 45.00 1.81 ± 0.41 0.33 ± 0.06 Veh/decitabine 0.1 mg/kg IP 13.6 ± 0.55 70.00 2.01 ± 0.41 0.31 ± 0.07 ER-876437 0.01 mg/kg/decitabine  12 ± 0.0 50.00 2.06 ± 0.23 0.32 ± 0.04 0.1 mg/kg PO ER-876437 0.1 mg/kg/decitabine 13.2 ± 0.84 65.00 2.28 ± 0.25 0.35 ± 0.1  0.1 mg/kg PO ER-876437 1 mg/kg/decitabine 14.2 ± 0.84 77.50 2.24 ± 0.32 0.34 ± 0.09 0.1 mg/kg PO ER-876437 1.0 mg/kg/Veh  8.4 ± 0.55 5.00 2.04 ± 0.15 0.32 ± 0.02 Veh: vehicle only ${*\%\mspace{14mu}{ILS}} = {\frac{\begin{matrix} {{{mean}\mspace{14mu}{survival}\mspace{14mu}{of}\mspace{14mu}{experimental}{\;\mspace{11mu}}{group}\mspace{14mu}({days})} -} \\ {{mean}\mspace{14mu}{survival}\mspace{14mu}{controls}\mspace{14mu}{group}\mspace{14mu}({days})} \end{matrix}}{{Mean}\mspace{14mu}{survival}\mspace{14mu}{of}\mspace{14mu}{control}\mspace{14mu}{group}\mspace{14mu}({days})} \times 100}$

TABLE 13 Statistical Analysis (Log Rank Test as per Prism GraphPad) Comparison P value Control vs 0.1 mg/kg decitabine PO 0.002 Control vs 0.1 mg/kg decitabine PO (8 hr.) 0.002 Control vs 0.1 mg/kg decitabine IP 0.002 Control vs ER-876437 alone 0.353 Decitabine 0.1 mg/kg PO vs. decitabine 0.1 mg/kg PO 0.6015 (8 hr.) decitabine 0.1 mg/kg PO vs. decitabine 0.1 mg/kg IP 0.0086 Control vs ER-876437 0.01 mg/kg/ 0.002 decitabine 0.1 mg/kg PO decitabine 0.1 mg/kg PO vs. ER-876437 0.1 mg/kg/ 0.649 decitabine 0.1 mg/kg PO decitabine 0.1 mg/kg PO vs. ER-876437 0.1 mg/kg/ 0.0368 decitabine 0.1 mg/kg PO decitabine 0.1 mg/kg PO vs. ER-876437 1 mg/kg/ 0.0048 decitabine 0.1 mg/kg PO decitabine 0.1 mg/kg IP vs. ER-876437 1 mg/kg/ 0.1729 decitabine 0.1 mg/kg PO ER-876437 0.01 mg/kg/decitabine 0.1 mg/kg PO vs. 0.014 ER-876437 0.1 mg/kg/decitabine 0.1 mg/kg PO ER-876437 0.1 mg/kg/decitabine 1 mg/kg PO vs. 0.0889 ER-876437 1 mg/kg/decitabine 0.1 mg/kg PO Conclusion:

Co-administration of ER-876437 at both 0.1 mg/kg and 1 mg/kg with 0.1 mg/kg decitabine PO enhanced survival compared to decitabine administered PO alone but not decitabine administered IP in the L1210 survival model in mice. The lowest dose tested (0.01 mg/kg) had no effect on enhancing survival of mice treated with 0.1 mg/kg decitabine when administered via PO. The two higher doses of ER-876437 in combination with decitabine had a slight dose response (p=0.09). The minimally effective dose of ER-976437 in this model was found to be 0.1 mg/kg.

There was no difference in survival of mice dosed with 0.1 mg/kg decitabine PO 2×/day qdx4 7 hours apart or 8 hours apart.

All publications or patent applications described herein are hereby wholly incorporated by reference.

Example VII Effect of ER-876437 on the Half-Life of Decitabine in the Presence of CDA in Tris-HCl Buffer at 37° C.

This example describes the effect of ER-876437 on the half-life (T₁₁₂) of decitabine (Eisai) in the presence of cytidine deaminase (CDA) in Tris-HCl buffer at 37° C.

Materials and Equipment

This Example employed a Phenomenex Luna C18(2) HPLC column (100 Å 4.6×250 mm 5 μm). The solvent delivery system employed an HPLC quaternary pump, low pressure mixing. An autosampler having a variable loop, 0.1 to 100 μL range and temperature controlled thermostat was used. The UV detector can employ a dual wavelength detector, a diode array detector, a variable wavelength detector or equivalent, and can be recorded using chromatographic software (e.g., Waters Empower 2 Build 2154, Agilent ChemStation software version A.09.03 or higher for HPLC or equivalent).

The analytical balance employed was capable of weighing±0.1 mg. Degassed HPLC grade water and degassed HPLC grade acetonitrile were used as solvents for the mobile phases.

Diluting solution used to make the below solutions was Tris-HCl (37° C., ph 7.4, Boston BioProducts). Diluting solution also served as the blank for the UV spectra.

Decitabine Standard Control: 0.2 mM decitabine control was prepared by weighing 2.6 mg of decitabine in a 10 mL volumetric flask. The flask was diluted to volume with Tris-HCl buffer stored at 37° C. and mixed by inversion. Solution was labeled as decitabine stock solution. 1.0 mL of decitabine stock solution was transferred to a 5 mL volumetric flask and diluted to volume with the diluting solution and mixed by inversion.

ER-876437 Standard Control: 0.4 mM ER-876437 control was prepared by weighing 5.2 mg of ER-876437 in a 10 mL volumetric flask. The flask was diluted to volume with Tris-HCl buffer stored at 37° C. and mixed by inversion. Solution was labeled as ER-876437 stock solution. 1.0 mL of ER-876437 stock solution was transferred to a 5 mL volumetric flask and diluted to volume with the diluting solution and mixed by inversion.

Decitabine with CDA: 1.0 mL of decitabine stock solution was transferred to a 5 mL volumetric flask. Approximately 2-3 mL of diluting solution was transferred to the flask. 0.125 mL of CDA solution was transferred to the flask and diluted to volume with diluting solution. The sample was mixed by inversion and injected into the HPLC immediately after preparing.

Decitabine with CDA and ER-876437: 1.0 mL of ER-876437 stock solution was transferred to a 5 mL volumetric flask. Approximately 2 mL of diluting solution was transferred to the flask. 0.125 mL of CDA solution was transferred to the flask. 1.0 mL of decitabine stock solution was transferred to the same flask and diluted to volume with diluting solution. The sample was mixed by inversion and injected into the HPLC immediately after preparing.

HPLC Parameters: The above standards and samples were run on an HPLC column using the parameters shown in Table 14.

TABLE 14 HPLC Parameters Column Temperature: 25° C. Autosampler Temperature: 37° C. Flow rate: 1.0 mL/min. Flow rate may be adjusted ±0.2 mL/min to obtain specified retention times. Gradient: Time, %-Solvent %-Solvent min A* B* Initial 96  4 10 96  4 20 75 25 25 75 25 Re-equilibration time 10 minutes Injection volume: 25 μL Needle Wash Solution: Use the diluting solution Detection: 205 nm UV Run Time: 25 minutes *Solvent A: water; solvent B: acetonitrile

The retention time for decitabine was found to be approximately 8 minutes; and the retention time of ER-876437 was found to be approximately 21.8 minutes.

Results and Discussion

TABLE 15 Summary of Results Solutions Estimated T_(1/2) Decitabine in Tris-HCl buffer at 37° C. 9 hours Decitabine with CDA in Tris-HCl buffer at 37° C. 23 minutes Decitabine with CDA and ER-876437-00 in Tris-HCl 9 hours buffer at 37° C.

The levels of decitabine, in the presence and absence of CDA, with or without ER-876437, in Tris-HCl buffer at 37° C. were measured by HPLC analysis using UV detection. The areas of the decitabine and ER-876437 peaks in the stability samples were measured and compared to the areas of the decitabine and ER-876437 standard controls, respectively. Results were reported as percent remaining of control.

Data was collected at 205 nm UV because decitabine and ER-876437 share this UV maximum. See FIG. 3. Results were captured every 35 minutes for 12 hours and intermittently thereafter due to the length of the analytical method. HPLC Chromatograms showing overlaid traces at specified time points are shown in FIGS. 4 and 5.

HPLC chromatograms in these figures are shown with a constant, additive offset for clarity. Although the bottom trace is shown starting at time=0.00 minutes, each successive chromatogram is arbitrarily shifted to the right of the previous chromatogram (by a constant amount of time) so as to avoid having the peaks overlap. The actual times associated with the peaks shown in these chromatograms can be realized by shifting the start of the chromatogram trace (at the left hand side) back to the vertical axis where time equals 0.00 minutes. Similarly, the actual UV absorption of any peak can be realized by shifting the baseline of the chromatogram to the position where mAU=0.00.

In the absence of CDA, the reduction of decitabine concentration to 50% was observed after 9 hours, while, in the presence of CDA, the concentration of decitabine was reduced to nearly 0% control after 2 hours and the T_(1/2) was estimated to be approximately 23 minutes. Addition of ER-876437 to the incubation mixture resulted in inhibition of the reaction with the reduction of decitabine concentration to 50% observed after 9 hours. The levels of ER-876437 were not affected after 12 hours exposure to CDA with decitabine. A summary of all the results are shown in FIG. 6.

The estimated T_(1/2) of decitabine in the presence of CDA in Tris-HCl buffer at 37° C. was found to be 23 minutes. ER-876437 nearly completely inhibited this effect resulting in the same T_(1/2) as decitabine alone in Tris-HCl buffer at 37 C (9 hours). 

1. A composition comprising decitabine and a compound of formula I:

wherein: one of R₁ and R₂ is F, and the other is selected from H and F; one of R₃ and R₄ is H, and the other is selected from H and OH; where ------- is a covalent bond or absent, and R₄ is absent when ------- is a covalent bond; or a pharmaceutically acceptable salt, a C₁₋₆ alkyl ester, or a C₂₋₆ alkenyl ester thereof.
 2. The composition of claim 1, wherein R₁ and R₂ are each F.
 3. The composition of claim 2, wherein said compound of formula I is a compound of formula II:

or a pharmaceutically acceptable salt, a C₁₋₆ alkyl ester, or a C₂₋₆ alkenyl ester thereof.
 4. The composition of claim 3 wherein said compound of formula II is a compound of formula VIII:

or a pharmaceutically acceptable salt, a C₁₋₆ alkyl ester, or a C₂₋₆ alkenyl ester thereof.
 5. The composition of claim 4 wherein said compound is a compound of formula VIII:


6. The composition of claim 2, wherein said compound of formula I is a compound of formula III:

wherein: one of R₃ and R₄ is H, and the other is selected from H and OH; or a pharmaceutically acceptable salt, a C₁₋₆ alkyl ester, or a C₂₋₆ alkenyl ester thereof.
 7. The composition of claim 1, wherein said compound of formula I is a compound of formula IV:

or a pharmaceutically acceptable salt, a C₁₋₆ alkyl ester, or a C₂₋₆ alkenyl ester thereof.
 8. The composition of claim 7, wherein said compound of formula IV is a compound of formula V:

or a pharmaceutically acceptable salt, a C₁₋₆ alkyl ester, or a C₂₋₆ alkenyl ester thereof.
 9. The composition of claim 1, wherein said compound of formula I is a compound of formula VI:

or a pharmaceutically acceptable salt, a C₁₋₆ alkyl ester, or a C₂₋₆ alkenyl ester thereof.
 10. The composition of claim 9, wherein said compound of formula VI is a compound of formula VII:

or a pharmaceutically acceptable salt, a C₁₋₆ alkyl ester, or a C₂₋₆ alkenyl ester thereof.
 11. A method of treating a cancer being treated with responsive to decitabine comprising: administering to a subject a composition comprising decitabine; and administering to a subject a composition comprising a compound of formula I:

wherein: one of R₁ and R₂ is F, and the other is selected from H and F; one of R₃ and R₄ is H, and the other is selected from H and OH; where is a covalent bond or absent, and R₄ is absent when is a covalent bond; or a pharmaceutically acceptable salt, a C₁₋₆ alkyl ester, or a C₂₋₆ alkenyl ester thereof.
 12. The method of claim 11, wherein said cancer is selected from the group consisting of hematological cancers and solid cancers.
 13. The method of claim 12, wherein said cancer is a hematological cancer selected from the group consisting of myelodysplastic syndrome, acute myeloid leukemia and chronic myeloid leukemia.
 14. The method of claim 12, where the cancer is a solid cancer selected from the group consisting of pancreatic cancer, ovarian cancer, peritoneal cancer, non small cell lung cancer, and metastatic breast cancer.
 15. The method of claim 11, wherein the compound is a compound of formula VIII:

or a pharmaceutically acceptable salt, a C₁₋₆ alkyl ester, or a C₂₋₆ alkenyl ester thereof.
 16. A pharmaceutical composition comprising (i) decitabine; (ii) a compound of formula I:

wherein: one of R₁ and R₂ is F, and the other is selected from H and F; one of R₃ and R₄ is H, and the other is selected from H and OH; where is a covalent bond or absent, and R₄ is absent when is a covalent bond; or a pharmaceutically acceptable salt, a C₁₋₆ alkyl ester, or a C₂₋₆ alkenyl ester thereof; and (iii) a pharmaceutically acceptable excipient.
 17. The pharmaceutical composition of claim 16, wherein R₁ and R₂ are each F.
 18. A pharmaceutical composition of claim 16 wherein the compound of formula I compound is a compound of formula VIII:

or a pharmaceutically acceptable salt, a C₁₋₆ alkyl ester, or a C₂₋₆ alkenyl ester thereof; and a pharmaceutically acceptable excipient.
 19. The method according to claim 11, wherein the composition comprising decitabine and the composition comprising a compound of formula I are simultaneously administered.
 20. The method according to claim 11, wherein the composition comprising decitabine and the composition comprising a compound of formula I are sequentially administered.
 21. The method of claim 13, wherein said hematological cancer is a myelodysplastic syndrome. 